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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452715Generated: October 27, 2026

4-(Chloromethyl)-1-methoxy-2-(trifluoromethyl)benzene → 2-(1-Benzofuran-5-yl)-5-[[4-methoxy-3-(trifluoromethyl)benzyl]thio]-1,3,4-oxadiazole

https://huagongshe.com/reaction/452715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)-1-methoxy-2-(trifluoromethyl)benzeneHCID 53429220—
ReactantHCID 178527940HCID 178527940—
Product2-(1-Benzofuran-5-yl)-5-[[4-methoxy-3-(trifluoromethyl)benzyl]thio]-1,3,4-oxadiazoleHCID 44590416100%

Reaction Steps

In the same manner as in Example 1 and using 5-(1-benzofuran-5-yl)-1,3,4-oxadiazole-2-thiol instead of 5-(benzothiazol-6-yl)-1,3,4-oxadiazole-2-thiol and 4-methoxy-3-(trifluoromethyl)benzyl chloride instead of 3-(trifluoromethyl)benzyl chloride, the title compound (yield 100%) was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-743fd860427b4af6a62a6e19eb8bbc32
Source noteuspto-grants-2013_07