会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 3. 发明专利
    • Improvements in and relating to the production and use of benzanthrone derivatives
    • GB348159A
    • 1931-04-30
    • GB3313129
    • 1929-10-31
    • SIDNEY THORNLEYJOHN THOMASSCOTTISH DYES LTD
    • C09B3/12
    • Benzanthrone derivatives.-Vat dyes are made by treating dibenzanthronyls or their substitution products with hydroxylamine or substances yielding hydroxylamine, followed by alkali fusion. In examples, (1) Bzl : Bzl1-dibenzanthronyl is sulphonated by treatment with oleum, the sulphonation mixture is treated with potassium hydroxylamine disulphonate or hydroxylamine hydrochloride in the presence of ferrous sulphate, and the product fused with caustic potash; the resulting dyestuff dyes in grey shades, (2) 2 : 21-dibenzanthronyl is similarly sulphonated, treated with potassium hydroxylamine disulphonate and fused with caustic potash; the product dyes in greenishgrey shades, (3) Bzl : Bzl1-dibenzanthronyl is treated with potassium hydroxylamine disulphonate in sulphuric acid with addition of ferrous sulphate, and the product fused with caustic potash; the resulting dyestuff dyes in blue-grey shades, (4) chlorinated Bzl : Bzl1-dibenzanthronyl (containing 16,7 per cent chlorine) is sulphonated with oleum, treated with hydroxylamine hydrochloride in the sulphonation mixture, and the product fused with caustic potash; the resulting dyestuff dyes in greenish-grey shades, and (5) chlorinated 2 : 21-dibenzanthronyl (16 per cent chlorine) is treated with potassium hydroxylamine disulphonate in sulphuric acid and fused with caustic potash; the product dyes in grey shades. The products may be alkylated as described in Specification 348,160.
    • 8. 发明专利
    • Improvements in and relating to the production and use of benzanthrone derivatives
    • GB367462A
    • 1932-02-25
    • GB2536930
    • 1930-08-25
    • ROBERT FRASER THOMSONIAN BLOHM ANDERSONSIDNEY THORNLEYICI LTD
    • C07C45/65C07C45/67
    • Benzanthrone derivatives containing selenium are made by the interaction of benzanthrone or its substitution products with selenium or a selenium compound. The products may be treated with acid or alkaline condensing agents, or nitrating (followed by reduction if desired), halogenating, sulphonating, or oxidizing agents, or they may be condensed with alkyl or aryl halides or subjected to heat treatment, further products being thereby obtained. In examples (1) benzanthrone is treated with selenium dioxide in sulphuric acid to give a product containing selenium; on alkali-fusion this gives a vat dye dyeing in blue shades; (2) Bz1 : Bz1 -dibenzanthronyl selenide is obtained by treating Bz1-chlorbenzanthrone (a) with selenium or selenium dioxide in tetrahydronaphthalene in presence of sodium acetate, or (b) with selenium and calcium hydroxide in methylated spirit, with or without a copper catalyst; other acid absorbers, e.g. quicklime, barium hydroxide, sodium phosphate or sodium acetate may be used instead of calcium hydroxide; (3) Bz1 : Bz1 -dibenzanthronyl selenide is treated with chlorine in nitrobenzene in presence of a trace of iodine; the product, according to one of the Provisional Specifications, is a mixture of benzanthrone and chlorbenzanthrone; (4) Bz1 : Bz1 -dibenzanthronyl selenide is brominated at room temperature; the product appears to be a dibromobenzanthrone; (5) Bz1 : Bz1 -dibenzanthronyl selenide on alkali-fusion, or on treatment with aluminium chloride in pyridine, yields isodibenzanthrone; (6) Bz1 : Bz1 -dibenzanthronyl selenide is oxidized with hydrogen peroxide in sulphuric acid; the product, on alkali-fusion, dyes in a similar shade to that given by isodibenzanthrone; (7) Bz1 : Bz1 -dibenzanthronyl selenide is nitrated in the presence or absence of sulphuric acid or in nitrobenzene; one of the products is a tetranitro derivative which, on alkali-fusion, gives a vat dye dyeing in grey shades; (8) Bz1 : Bz1 -dibenzanthronyl selenide is sulphonated; (9) Bz1-benzanthronyl hydrogen selenide is obtained by treating Bz1-chlorbenzanthrone with selenium and caustic soda in methylated spirit; on treatment with dimethyl sulphate or iodobenzene the corresponding methyl- and phenyl-selenides are obtained: the latter yields isodibenzanthrone on alkali-fusion; (10) Bz1 : Bz1 -dibenzanthronyl selenide is obtained from Bz1-benzanthronyl hydrogen selenide (a) by heating to 300 DEG C, (b) by heating with copper and nitrobenzene, (c) by heating with alcohol with addition of copper and lime, (d) by heating with selenious acid in nitrobenzene, or (e) by heating in sulphuric acid; (11) dichlorbenzanthrone (made by chlorinating Bz1-chlorbenzanthrone with sulphuryl chloride in nitrobenzene in presence of iodine) is treated with selenium to give a chlorinated dibenzanthronyl selenide, which, on alkali-fusion, gives a dye of the isodibenzanthrone type, and (12) nitro- and methoxy-Bz1-chlorbenzanthrones (examples (1) and (4) of Specification 256,281, [Class 2 (iii), Dyes &c.], on similar treatment yield amino-and methoxy-Bz1 : Bz1 -dibenzanthronyl selen ides, which also give dyes of the isodibenzanthrone type on alkali-fusion.
    • 9. 发明专利
    • Improvements in and relating to the production and use of benzanthrone derivatives
    • GB348160A
    • 1931-04-30
    • GB3313229
    • 1929-10-31
    • SIDNEY THORNLEYROBERT FRASER THOMSONJOHN THOMASSCOTTISH DYES LTD
    • C09B3/24
    • Benzanthrone derivatives.-The dyes obtained by treating benzanthrone or dibenzanthronyls or their substitution products with hydroxylamine or substances yielding hydroxylamine (such as potassium hydroxylamine mono- and di-sulphonates), followed by alkali fusion, are treated with alkylating or aralkylating agents; the products are usually faster than the original dyes. In examples (1) the product obtained from benzanthrone by sulphonation, treatment with hydroxylamine or potassium hydroxylamine disulphonate, and caustic potash fusion, is reduced with sodium bisulphite in sulphuric acid and methylated with dimethylsulphate in nitrobenzene; the product dyes cotton in bluish-grey shades, (2) the products of examples 1, 2, and 3 of Specification 348,159, are treated with dimethylsulphate to yield products dyeing in blue to grey shades, (3) the parent material used in example 1 is benzylated by means of benzyl chloride; the product dyes in grey-blue shades, (4) the product obtained by sulphonating chlorinated Bzl : Bzl1-bibenzanthronyl (containing 16,7 per cent chlorine), treating with hydroxylamine hydrochloride and alkali fusion is methylated with dimethylsulphate; the product dyes in blue-grey shades, (5) the product obtained by treating chlorinated 2 : 21-dibenzanthronyl (containing 16 per cent chlorine) with potassium hydroxylamine disulphonate and alkali fusion is methylated with dimethylsulphate; the product dyes in blue-grey shades, and (6) the product obtained by sulphonating Bzl-chlorbenzanthrone, treating with hydroxylamine hydrochloride and alkali fusion is methylated with dimethylsulphate; the product dyes in violet shades.