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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579110Generated: October 31, 2026

Pyridine → HCID 21484429, compound

https://huagongshe.com/reaction/1579110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21484478HCID 21484478—
SolventWaterHCID 962—
ProductHCID 21484429HCID 21484429—

Reaction Steps

33.1 g of β-(m-cyclohexyl-phenyl)-ethanol are mixed with 13.3 ml of absolute pyridine. 12.5 ml of thionyl chloride are added dropwise to this mixture, whilst cooling with ice. Thereafter the reaction mixture is slowly heated to 100°-110°C and is kept at this temperature for 2 hours. The reaction solution is again cooled to room temperature, 29 ml of water are added and the whole is extracted with a mixture of ether and chloroform. The organic phase is washed twice with 2 N sodium carbonate solution, three times with 2 N hydrochloric acid and finally once with 2 N sodium carbonate solution, dried over sodium sulphate, filtered and evaporated. The residue, a brown oil, is distilled in a high vacuum. Hereupon, β-(m-cyclohexyl-phenyl)-ethyl chloride is obtained as a light yellow oil of boiling point 103°-8°C/0.1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03940434
Source datasetuspto-grants-1976_02
ORD IDord-4c7833b96e6c4ea5949923b41a2ddc39
Source noteuspto-grants-1976_02