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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22433Generated: October 25, 2026

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

https://huagongshe.com/reaction/22433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantSodium ethoxideHCID 2723922—
Reactant2-(6-Bromohexyloxy)-5-methyl-1,3-benzenedicarboxaldehydeHCID 19930264—
SolventEthanolHCID 702—
Product2-(6-Benzylthiohexyloxy)-5-methyl-1,3-benzenedicarboxaldehydeHCID 19930289—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428065
Source datasetuspto-grants-1995_06
ORD IDord-7f6483fff6624318bcdbcd4153c44add
Source noteuspto-grants-1995_06