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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453128Generated: November 1, 2026

Sodium Thiosulfate → 4-Bromo-2-(2,2,2-trifluoroethyl)phenol

https://huagongshe.com/reaction/1453128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant2-(2,2,2-Trifluoroethyl)phenolHCID 17796921—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventChloroformHCID 6212—
Product4-Bromo-2-(2,2,2-trifluoroethyl)phenolHCID 58762562187.3%

Reaction Steps

Tetrabutylammonium tribromide (6.56 g) was dissolved in chloroform (50 ml) and added dropwise to a solution of 2-(2,2,2-trifluoroethyl)phenol (2.4 g) in chloroform (50 ml). The reaction mixture was stirred at room temperature for 2 hrs, after which time 5% sodium thiosulfate solution (100 ml) was added and the resultant stirred for 30 mins. The mixture was then partitioned between dichloromethane (100 ml) and 1N HCl (200 ml). The organics were separated and dried over magnesium sulfate. The solvent was then removed in vacuuo, the crude residue was then purified by column chromatography on silica gel eluting with 90:10 hexanes:ethl acetate to afford the title compound as a yellow oil (3.24 g). 1H NMR (CDCl3): δ 3.50 (q, J=21.48 Hz 2H), 6.70 (d, J=2.54 Hz, 1H), 7.32 (d, J=2.54 Hz, 1H), 7.45 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473790B2
Source datasetuspto-grants-2009_01
ORD IDord-513f4e96298c4dc5833fb72c9ae304d1
Source noteuspto-grants-2009_01