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HRID 22433作成日:2026年10月25日

Benzyl mercaptan → 2-(6-Benzylthiohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde

https://huagongshe.com/reaction/22433

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl mercaptanHCID 7509—
反応物Sodium ethoxideHCID 2723922—
反応物2-(6-Bromohexyloxy)-5-methyl-1,3-benzenedicarboxaldehydeHCID 19930264—
溶媒EthanolHCID 702—
生成物2-(6-Benzylthiohexyloxy)-5-methyl-1,3-benzenedicarboxaldehydeHCID 19930289—

反応手順

A solution of sodium ethoxide (69 mg sodium, 3 mmol in ethanol 1 ml) was added to a stirred suspension of 2-(6-bromohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde (0.98 g, 3 mmol) and benzyl mercaptan (0.35 g, 3 mmol) in ethanol (10 ml) at room temperature under nitrogen. After 1 hour evaporated, water (10 ml) and 2M sodium hydroxide (2 ml) added and extracted with diethyl ether (10 ml). The extracts were washed with water, dried, filtered and evaporated to an oil (1.12 g). Chromatography on silica eluting with dichloromethane gave 2-(6-benzylthiohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428065
出典データセットuspto-grants-1995_06
ORD IDord-7f6483fff6624318bcdbcd4153c44add
出典メモuspto-grants-1995_06