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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422179Generated: October 26, 2026

(3-Benzyloxy-5-trifluoromethylthien-2-yl)-carboxylic acid → 3-Benzyloxy-5-trifluoromethylthiophen

https://huagongshe.com/reaction/1422179

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Benzyloxy-5-trifluoromethylthien-2-yl)-carboxylic acidHCID 11426602—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
Product3-Benzyloxy-5-trifluoromethylthiophenHCID 1118447071%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 1F (14.5 g) and quinoline (50 ml) was treated with copper powder (4.57 g) and heated to 150 ° C. The reaction mixture is heated for 25 minutes at 150° C. and cooled to room temperature. The mixture was filtered and washed with water. Aqueous quinoline was acidified with 6N HCl (pH=2) and extracted with diethyl ether twice. The combined organic phases were washed with water and dried. The mixture was concentrated and the residue was chromatographed to yield a yellow liquid (8.74 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080861
Source datasetuspto-grants-2000_06
ORD IDord-03359913941640338a5dac1b94a9abf9
Source noteuspto-grants-2000_06