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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212081Generated: November 2, 2026

Triethylamine → HCID 21963748, compound

https://huagongshe.com/reaction/2212081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10997188HCID 10997188—
ReactantHCID 21963772HCID 21963772—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 21963748HCID 21963748—

Reaction Steps

A solution of 3-(1-benzenesulphonylcyclopent-3-enyl)propan-1-ol (56 mg, 0.21 mmol) and triethylamine (41 μL, 0.29 mmol) in dichloromethane (5 ml) was cooled to 0° C. and treated with methanesulphonyl chloride (21 μL, 0.27 mmol). The mixture was allowed to warm to room temperature and stirred for 30 minutes, then diluted with water and extracted with ethyl acetate. The combined organic layers were dried (MgSO4) and concentrated in vacuo. The residue was dissolved in acetonitrile (5 ml), treated with 3,4-dimethyl-1,2,5,6-tetrahydropyridine (397 mg, 0.32 mmol) and potassium carbonate (58 mg, 0.42 mmol) and heated at 60° C. for 3 hours. The mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were dried (MgSO4) and concentrated in vacuo. The residue was purified by preparative thin layer chromatography, eluting with 5% methanol/dichloromethane, to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101892B2
Source datasetuspto-grants-2006_09
ORD IDord-0e6f2490dd494bd3b9b642b075fe5097
Source noteuspto-grants-2006_09