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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596303Generated: October 26, 2026

Water → 2-(3,5-Bis-trifluoromethyl-benzyloxymethyl)-biphenyl

https://huagongshe.com/reaction/1596303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant3,5-Bis(trifluoromethyl)benzyl alcoholHCID 122933—
Reactant2-(Chloromethyl)-1,1'-biphenylHCID 21972820—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product2-(3,5-Bis-trifluoromethyl-benzyloxymethyl)-biphenylHCID 1854650048.7%

Reaction Steps

To a solution of 1.53 g (6.26 mmol) (3,5-bis-trifluoromethyl-phenyl)-methanol in 15 ml N,N-dimethylformamide 0.30 g (7.52 mmol) sodiumhydride (60% dispersion in mineral oil) was added and the reaction mixture was stirred for 1 hr. After the addition of 1.27 g (6.26 mmol) 2-chloromethyl-biphenyl in 5 ml N, N-dimethylformamide at 0°, the reaction mixture was stirred for 3 hrs. at RT. The reaction mixture was distributed between 50 ml H2O, 50 ml brine and 50 ml CH2Cl2. The phases were separated, the aqueous layer washed twice with 50 ml CH2Cl2. The combined organic layers were dried (MgSO4), filtered and evaporated. The residue was purified by chromatography (SiO2, hexane/ethyl acetate 40:1) to give 1.25 g (47%) 2-(3,5-bis-trifluoromethyl-benzyloxymethyl)-biphenyl as a colorless oil, MS (EI):410 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291465B1
Source datasetuspto-grants-2001_09
ORD IDord-372e6c79c7f347d7a817c500db516933
Source noteuspto-grants-2001_09