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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084651Generated: November 1, 2026

Hydrochloric Acid → HCID 15754357, compound

https://huagongshe.com/reaction/1084651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15754307HCID 15754307—
SolventDimethylformamideHCID 6228—
ProductHCID 15754357HCID 1575435773.3%

Reaction Conditions

Temperature10 °C

Reaction Steps

A DMF suspension of 2.2 g (0.05 mol) of sodium hydride (about 60% in oil) was cooled with ice water, and 5.1 g (0.05 mol) of ethyl mercaptan was dropwise added thereto at a temperature not higher than 10° C. under stirring. The reaction mixture was returned to room temperature and left to stand for about 30 minutes. Then, a DMF solution of 15.7 g (0.04 mol) of 1-(3,5- dichloro-4-methoxy-α,α-dimethylbenzyl)-4-methyl-3-phenyl- 3-pyrrolin-2-one (Compound No. 143) prepared in Example 2, was added thereto. The solution was heated at about 80° C. and reacted for three hours. After completion of the reaction, the reaction solution was poured into a large amount of ice water, acidified with a 10% hydrochloric acid aqueous solution and then extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The solid thereby obtained was washed with isopropyl ether to obtain 11.0 g (yield: 73.3%) of the desired compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05006157
Source datasetuspto-grants-1991_04
ORD IDord-5b9e44ac2f1445b89570066876c83131
Source noteuspto-grants-1991_04