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HRID 376229作成日:2026年10月26日

p-Toluenesulfonic acid → Ethyl 2-[5,7-di(t-butyl)benzothiazolyl]acetate

https://huagongshe.com/reaction/376229

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物3,5-Bis(tert-butyl)benzoic acidHCID 85339—
反応物3,5-Di(t-butyl)-2-mercaptoanilineHCID 12087014—
溶媒MethanolHCID 887—
生成物Ethyl 2-[5,7-di(t-butyl)benzothiazolyl]acetateHCID 19360973—

反応手順

A mixture of 40 g of 3,5-di(t-butyl)-2-mercaptoaniline [prepared according to a literature procedure from 3,5-di(t-butyl)benzoic acid] and 75 mL of ethyl 3-(trimethoxy)propionate in 1.2 L of methanol containing 1.5 g of p-toluenesulfonic acid was stirred at r.t. for 18 h. Excess methanol was removed by rotary evaporation. The precipitated the solid was filtered and washed with cold methanol. The crude product was purified by flash chromatography on silica gel and eluted with heptane to give 20 g of ethyl 2-[5,7-di(t-butyl)benzothiazolyl]acetate. The latter was refluxed with 16 g of 1,1,7,7-tetramethyl-8-hydroxy-9-formyljulolidine in 200 mL of acetonitrile containing 4 mL of piperidine for 18 h. The reaction mixture was cooled and the precipitated bright orange solid was filtered to give 13 g of the desired dye C-545TB: m.p. 275-276° C.; Tg=140° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06020078
出典データセットuspto-grants-2000_02
ORD IDord-7b439c4485154a7787245cc35d75960c
出典メモuspto-grants-2000_02