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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476533Generated: October 29, 2026

Ethanethiol → Methyl 2-chloro-3-ethylthiomethyl-4-methanesulfonylbenzoate

https://huagongshe.com/reaction/476533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-bromomethyl-2-chloro-4-methylsulfonylbenzoateHCID 10969914—
SolventChloroformHCID 6212—
ProductMethyl 2-chloro-3-ethylthiomethyl-4-methanesulfonylbenzoateHCID 1513283998.6%

Reaction Steps

To 100 ml of tetrahydrofuran, 1.3 g of ethanethiol and 1.5 g of potassium carbonate and then 4.4 g of methyl 3-bromomethyl-2-chloro-4-methanesulfonylbenzoate were added, and the mixture was stirred for 1 day at room temperature. Then, the mixture was stirred further for 1 hour at a temperature of from 50° to 60° C. After cooling, chloroform was added thereto, and the mixture was washed with a dilute potassium carbonate aqueous solution. The chloroform layer was separated and dried. Then, the solvent was distilled off to obtain 4.1 g of methyl 2-chloro-3-ethylthiomethyl-4-methanesulfonylbenzoate as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885022
Source datasetuspto-grants-1989_12
ORD IDord-dfd71aef5be84e7288d737f2d2554e31
Source noteuspto-grants-1989_12