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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031669Generated: October 30, 2026

Methanethiol → HCID 14722454, compound

https://huagongshe.com/reaction/1031669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantHCID 10621601HCID 10621601—
SolventDichloromethaneHCID 6344—
ProductHCID 14722454HCID 1472245447.4%

Reaction Steps

In 50 ml of methylene chloride were dissolved 2.06 g of 3-bromo-2,3-dihydro-7-methylsulfonylamino-6-phenoxy-4H-1-benzopyran-4-one and 480 mg- of methylmercaptan. Thereto was added 2.02 g of triethylamine at 0°-5° C. The mixture was stirred for 1 hour at room temperature. The reaction mixture was introduced into 30 ml of water. The organic layer was separated, washed with water, and dried with anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by a column chromatography (eluant: a 50 : 1 mixture of toluene and ethyl acetate) to obtain 900 mg (yield: 47.4%) of 2,3-dihydro-7-methylsulfonylamino-3-methylthio-6-phenoxy-4H-1-benzopyran-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954518
Source datasetuspto-grants-1990_09
ORD IDord-9d784d8d52ff429ba9cede2d3ed95035
Source noteuspto-grants-1990_09