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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665968Generated: November 1, 2026

Epichlorohydrin → HCID 57508926, compound

https://huagongshe.com/reaction/1665968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 135968114HCID 135968114—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 57508926HCID 5750892699.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 4-[5-(5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-[1,2,4]oxadiazol-3-yl]-2,6-dimethyl-phenol (35 mg, 1.18 mmol) in isopropanol (17 mL) is treated with 2 N aq. NaOH (8.6 mL) followed by epichlorohydrine (660 mg, 7.14 mmol). The mixture is stirred at 50° C. for 18 h before it is diluted with water and extracted twice with EA. The combined organic extracts are dried over Na2SO4, filtered, evaporated and dried to give 3-(3,5-dimethyl-4-oxiranylmethoxy-phenyl)-5-(5,5-dimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-[1,2,4]oxadiazole (480 mg) as a pale yellow oil; LC-MS: tR=1.24 min, [M+1]+=411.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039644B2
Source datasetuspto-grants-2011_10
ORD IDord-b551eb8bdc4d441a9cf81a083744d8c3
Source noteuspto-grants-2011_10