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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649613Generated: October 28, 2026

Imidazole → HCID 57106152, compound

https://huagongshe.com/reaction/649613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 14100235HCID 14100235—
SolventDichloromethaneHCID 6344—
ProductHCID 57106152HCID 57106152—

Reaction Steps

To a suspension of 4.08 g of imidazole and 30 ml of dry methylene chloride, 1.78 g of thionyl chloride was added with ice-cooling. After stirring the reaction mixture for 30 minutes, 2.58 g of 2-benzylthio-2'-hydroxyacetophenone was added, followed by further stirring at room temperature for 2 hours. Ice water was added to the reaction mixture, followed by extraction with methylene chloride. The organic, i.e., methylene chloride layer was washed with water, dried over magnesium sulfate and then concentrated. The residue was dissolved in chloroform and was then subjected to chromatography on a silica gel column. Upon concentration of the resultant eluate, there were obtained 180 mg of Isomer A (m.p. 196°-198° C.; Compound 1) and 1.0 g of Isomer B (m.p. 136.5°-138° C.; Compound 2) of 1-(2-hydroxyphenyl)-1-imidazolyl-2-benzylthioethylene (in formula (I), R1, R2, R3 =H, R4 =--SCH2C6H5), both, as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04740601
Source datasetuspto-grants-1988_04
ORD IDord-45870dc4ab8749cd80491062cca3dff3
Source noteuspto-grants-1988_04