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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707532Generated: October 31, 2026

Pyridine → HCID 178445619, compound

https://huagongshe.com/reaction/1707532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178445651HCID 178445651—
ProductHCID 178445619HCID 17844561990.9%

Reaction Steps

37 g (0.22 mol) of trans-4-butylcyclohexylmethanol and 18 g (0.23 mol) of anhydrous pyridine were given dropwise addition of 32 g (0.27 mol) of SOCl2 in an ice water bath while stirring, and then stirred for 3 hours at 105°-110° C. with a mantle heater. The reactant was cooled to room temperature, poured into a beaker containing concentrated HC1 and ice, the oily layer was taken off, the water layer was extracted with chloroform, combined with the oily layer and washed with 10% HCl and water. The chloroform was extracted, and the remaining oily substance was distilled under reduced pressure (b. p. 80° C./3 mmHg) to obtain 38 g (0.20 mol) of trans-4-butylcyclohexylchloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354502
Source datasetuspto-grants-1994_10
ORD IDord-a4ea0d41ee234719bae1dd8bf6bd9819
Source noteuspto-grants-1994_10