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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863032Generated: October 31, 2026

Thionyl Chloride → HCID 12782362, compound

https://huagongshe.com/reaction/1863032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 12298104HCID 12298104—
SolventDichloromethaneHCID 6344—
ProductHCID 12782362HCID 1278236261.7%

Reaction Steps

To 4.5 parts of sulfinyl chloride is added dropwise a mixture of 13 parts of N-[1-(2-hydroxy-2-phenylethyl)-4-(methoxymethyl)-4-piperidinyl]-N-phenylpropanamide hydrochloride and 260 parts of dichloromethane. Upon completion, the whole is stirred and refluxed for a few hours. The reaction mixture is cooled and the solvent is evaporated. The residue is taken up in 2-propanone. The mixture is filtered and the filtrate is treated with activated charcoal. The latter is filtered off and the filtrate is evaporated. The residue is crystallized from a mixture of 2-propanone and 2,2'-oxybispropane. The product is filtered off and dried, yielding 9.2 parts (61.7%) of N-[1-(2-chloro-2-phenylethyl)-4-(methoxymethyl)-4-piperidinyl]-N-phenylpropanamide monohydrochloride; mp. 145.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167574
Source datasetuspto-grants-1979_09
ORD IDord-d8ce5654b3ae4bceb72d5cf1ccc98cff
Source noteuspto-grants-1979_09