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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704594Generated: October 30, 2026

Ethanethiol → HCID 20072961, compound

https://huagongshe.com/reaction/704594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantHCID 10402623HCID 10402623—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 20072961HCID 20072961—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.56 g of sodium methylate is MeOH (5 ml), cooled at 0° C., was treated with 0,71 ml of ethanethiol (CH3CH2SH). After 10 minutes, a solution of 3 g of 2-(4-methoxyphenoxymethyl)-3-α-chloroacetyl-1,3-thiazolidine in 10 ml MeOH was dropped into the mixture. After 30 minutes, the solvent was removed under reduced pressure and the residue was partitioned between 30% NaH2PO4 and ethyl acetate. The organic phase was washed with water, dried over Na2SO4 and concentrated to dryness to yield 2,9 g of 2-(4-methoxyphenoxymethyl)-3-ethylmercaptoacetyl- 1,3-thiazolidine after crystallization from isopropyl ether, m.p. 98°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988701
Source datasetuspto-grants-1991_01
ORD IDord-66438709f87648e297d9ba2eabe96081
Source noteuspto-grants-1991_01