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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238301Generated: October 30, 2026

Triethylamine → 5-(3-Chloroprop-1-EN-1-YL)-2-(4-fluorophenyl)pyridine

https://huagongshe.com/reaction/238301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(6-(4-Fluorophenyl)pyridin-3-yl)prop-2-en-1-olHCID 68821919—
SolventDichloromethaneHCID 6344—
Product5-(3-Chloroprop-1-EN-1-YL)-2-(4-fluorophenyl)pyridineHCID 6882210299.1%

Reaction Steps

436 mg (3.8 mmol) of methanesulfonyl chloride were slowly added at room temperature to 513 mg (2.24 mmol) of 3-(6-(4-fluorophenyl)pyridin-3-yl)prop-2-en-1-ol and 679 mg (6.71 mmol) of triethylamine in 20 ml of dichloromethane. The mixture was stirred at room temperature for 6 h and extracted with a sodium hydrogencarbonate solution. The organic phase was evaporated to yield 550 mg of the title compound. MS: M+H+=248.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642620B2
Source datasetuspto-grants-2014_02
ORD IDord-8d5d00b21e0943be82c2cad4c83c6aea
Source noteuspto-grants-2014_02