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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082676Generated: October 31, 2026

Thionyl Chloride → HCID 20360379, compound

https://huagongshe.com/reaction/2082676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 20360357HCID 20360357—
SolventTolueneHCID 1140—
ProductHCID 20360379HCID 2036037940%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a stirred and cooled (5°-10° C) mixture of 60 parts of 2-[{phenyl[3-(trifluoromethyl)phenyl]methyl}amino]-ethanol and 540 parts of methylbenzene are added dropwise 40 parts of sulfinyl chloride. Upon completion, stirring is continued first till room temperature is reached and further overnight at reflux temperature. The reaction mixture is concentrated to one third its volume. After cooling to 10° C, the solid product is filtered off, washed with 2,2'-oxybispropane and dried in vacuo at 75° C, yielding 28.5 parts (40%) of N-(2-chloroethyl)-α-phenyl-3-(trifluoromethyl)benzenemethanamine hydrochloride; mp. 187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082755
Source datasetuspto-grants-1978_04
ORD IDord-dd63033918274148833049e4b202a1d6
Source noteuspto-grants-1978_04