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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275467Generated: November 2, 2026

Ethanethiol → HCID 22118376, compound

https://huagongshe.com/reaction/1275467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22118429HCID 22118429—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 22118376HCID 2211837675%

Reaction Steps

A methanolic solution of 0.8 g (4 mmol, 3 eq.) containing about 28 wt % sodium methoxide was diluted with 5 ml of anhydrous methanol, and 0.5 ml (6.8 mmol, 1.5 eq.) of ethanethiol was added. The mixture was stirred at room temperature for 5 minutes, and then 0.5 g (1.3 mmol) of 3,3,5-trimethyl-4-methanesulfonyloxy-6-ethoxycarbonylthiochroman-1,1-dioxide was added. The mixture was refluxed for 8 hours, and allowed to stand at room temperature for 5 days. The reaction mixture was diluted with 100 ml of ethyl acetate and washed with 50 ml of water twice, and an aqueous layer was separated and cooled in an ice bath. The aqueous layer was acidified with 5 wt % hydrochloric acid and extracted with 100 ml of ethyl acetate, and an organic layer was dried over sodium sulfate. The solvent was distilled off, and the residue was dried under reduced pressure to give 0.32 g (yield 75%) of a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159904
Source datasetuspto-grants-2000_12
ORD IDord-9d9ce6a30c3148918bc78a8bc8e9295b
Source noteuspto-grants-2000_12