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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382008Generated: October 30, 2026

Aluminum → 2,4-Di-tert-butyl-6-(trifluoromethyl)phenol

https://huagongshe.com/reaction/1382008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminumHCID 5359268—
ReactantHCID 14343498HCID 14343498—
SolventWaterHCID 962—
Product2,4-Di-tert-butyl-6-(trifluoromethyl)phenolHCID 1434350883.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

A strip of aluminum foil weighing 267 mg (9.9 mmol) was amalgmated by immersion in a solution of 2% mercuric chloride in water for 15 seconds, washed with absolute ethanol followed by diethyl ether, cut into small pieces, and added to a solution of 400 mg (0.99 mmol) of 4,6-di-tert-butyl-2-triethylsiloxy-2-trifluoromethyl-3,5-cyclohexadien-1-one in 25 mL of 10% water 90% tetrahydrofuran. The resulting mixture was heated at 70° C. for 1.5 hours, allowed to cool to room temperature, and filtered. The filter cake was washed with 10 mL of tetrahydrofuran. Concentration of the combined filtrates gave a residue which was poured into 25 mL of water. The aqueous mixture was extracted with three 10 mL portions of dichloromethane. Combination, drying and concentration of the organic layers gave a residue which was purified by PTLC (one 2 mm silica gel plate eluted with petroleum ether), affording 226 mg (83% yield) of 2,4-di-tert-butyl-6-trifluoromethylphenol as a colorless liquid: 1H NMR (CDCl3)δ1.31 (s, 9H), 1.45 (s, 9H), 5.56 (q, 1H, JHF =4Hz), 7.39 (d, 1H, J=2Hz), 7.54 (d, 1H, J=2Hz); IR (neat) 3624, 2959, 2906, 2868, 1481, 1458, 1448, 1363, 1340, 1263, 1251, 1170, 1126, 1097, 887, 694 cm-1 ; mass spectrum (70 eV) m/z (relative intensity) 274 (20, M+), 259 (100), 239 (68), 98 (20), 57 (22), 41 (34).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04804773
Source datasetuspto-grants-1989_02
ORD IDord-4fabd940763e4ef498d0c5448c3d85f8
Source noteuspto-grants-1989_02