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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863033Generated: October 31, 2026

Thionyl Chloride → HCID 13676766, compound

https://huagongshe.com/reaction/1863033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 13676764HCID 13676764—
SolventDichloromethaneHCID 6344—
ProductHCID 13676766HCID 1367676685%

Reaction Steps

14 Parts of sulfinyl chloride are stirred and there is added dropwise a solution of 37 parts of N-[1-(2-hydroxypropyl)-4-(methoxymethyl)-4-piperidinyl]-N-phenylpropanamide monohydrochloride in 360 parts of dichloromethane. Upon completion, stirring is continued overnight at reflux temperature. The reaction mixture is evaporated and the residue is suspended in 2-propanone. The product is filtered off and dried, yielding 31.5 parts (85%) of N-[1-(2-chloropropyl)-4-(methoxymethyl)-4-piperidinyl]-N-phenylpropanamide monohydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167574
Source datasetuspto-grants-1979_09
ORD IDord-0fa4015a350647c6a901f636bc7cdcea
Source noteuspto-grants-1979_09