Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387070Generated: November 2, 2026

Ethanethiol → HCID 21182697, compound

https://huagongshe.com/reaction/1387070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium BicarbonateHCID 516892—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 10746430HCID 10746430—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 21182697HCID 2118269757%

Reaction Steps

4-[3-Bromo-4-[(1-pyrrolidinyl)methyl]phenyl 6-methoxy-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl ketone (34 mg; 0.055 mmol) (Part D) was dissolved in dichloroethane (5 mL) in a flame-dried, argon-filled flask, and cooled in an ice-water bath. Ethanethiol (0.16 mL; 2.2 mmol) was added, followed by 0.15 g (1.1 mmol) of aluminum chloride. The resultant slurry was stirred in the cold for 2 h. Saturated aqueous sodium bicarbonate (20 mL) was added, and stirring was continued for 2 h. Extraction was carried out with EtOAc (4×25 mL) and the combined organics were washed with brine and dried by passage through sodium sulfate. The product was isolated as a yellow oil (19 mg; 57% yield) by flash chromatography on silica gel, eluting with a gradient of EtOAc(100-90%)/Et3N(0-5%)/MeOH(0-5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-e694206fd4d540e4bd91676235ffe057
Source noteuspto-grants-2001_07