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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069207Generated: October 26, 2026

Dichloromethane → HCID 12972351, compound

https://huagongshe.com/reaction/1069207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTin tetrachlorideHCID 24287—
Reactant2,3-Dimethyl-5-benzylthiopheneHCID 10241963—
SolventWaterHCID 962—
ProductHCID 12972351HCID 1297235188%

Reaction Steps

Tin tetrachloride (4.6 mL, 71.76 mmol) was added dropwise over a 10 minute period to a stirred, −78° C. solution of 2-benzyl-4,5-dimethylthiophene (6.6 g, 32.62 mmol), anisoyl chloride (5.90 g, 34.6 mmol) and dichloromethane (120 mL) under a dry nitrogen atmosphere. After 5 hours at −78° C., the reaction mixture was slowly warmed to room temperature over a 2 h period. The reaction mixture was added to water and extracted with ether. The ether extract was washed with sat. aq. sodium bicarbonate and brine. The solvent was removed and the resultant solid was triturated with ether to give the title compound as a off-white solid (9.62 g, 88%): mp 85-86° C.: NMR (CDCl3); δ7.80 (ddd, J=8, 8, 1 Hz, 2H), 7.24-7.10 (m, 5H), 7.92 (ddd, J=8, 8, 1 Hz, 2H), 3.93 (s, 2H), 3.88 (s, 3H), 2.28 (s, 3H), 1.90 (s, 3H); MS (EI): 336 (100%, MI); Anal. Calc. for C21H20O2S: C, 74.97; H, 5.99; N, 0.00. Found: C, 75.11; H, 6.02; N, 0.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251936B1
Source datasetuspto-grants-2001_06
ORD IDord-08dc99a3b1694a4c85a4671b52bf7e60
Source noteuspto-grants-2001_06