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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534753Generated: November 4, 2026

Benzyl mercaptan → HCID 57201698, compound

https://huagongshe.com/reaction/1534753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantPotassium hydrideHCID 82127—
Reactant1-Methylethyl 3-methyl-2-nitrobenzoateHCID 52448870—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57201698HCID 57201698—

Reaction Steps

To a stirred suspension of dry tetrahydrofuran (125mL) and 35% potassium hydride in oil (6.3 g) was slowly added benzyl mercaptan (6.1 mL) at 0° C. under an inert atmosphere. After 15 minutes, 3-methyl-2-nitrobenzoic acid, 1-methylethyl ester (11.23 g) was added and the resulting mixture was stirred at room temperature overnight. The reaction mixture was partitioned between 6N sodium hydroxide (25 mL) and ethyl acetate (150 mL). The organic phase was dried over magnesium sulfate, filtered, concentrated, and chromatographed on silica gel eluted with 5% ethyl acetate in hexanes to give 13.7 g of the title compound as a yellow oil, nD 1.5642.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05090993
Source datasetuspto-grants-1992_02
ORD IDord-23829148d39d40df96058b75d1170e73
Source noteuspto-grants-1992_02