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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422180Generated: October 26, 2026

Carbon Tetrachloride → 4-Hydroxy-2-(trifluoromethyl)thiophene

https://huagongshe.com/reaction/1422180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantTrimethylsilyl iodideHCID 85247—
Reactant3-Benzyloxy-5-trifluoromethylthiophenHCID 11184470—
SolventWaterHCID 962—
Product4-Hydroxy-2-(trifluoromethyl)thiopheneHCID 11084273—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1G (7.75 g) and tetrachloromethane (50 ml) was treated with iodotrimethylsilane (12.30 ml) and heated to 60 ° C. for 12 hours. The reaction mixture was stirred at room temperature for 12 hours. Water (50 ml) was added and the resulting reaction mixture was extracted with dichloromethane three times. The combined organic phases were washed with water and dried. The crude reaction mixture was eluted through hexane (100 g/silica gel) to remove benzyliodide and then with diethyl ether. The ether phases were concentrated and distilled in vacuo to give the product (3.33 g, 74% having point of 65-66 ° C. at 4 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080861
Source datasetuspto-grants-2000_06
ORD IDord-3e1b8cadc204409b8117e0e4ceb56067
Source noteuspto-grants-2000_06