HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267512Generated: October 25, 2026
Water → 2-(3,5-Bis-trifluoromethyl-benzyloxymethyl)-biphenyl
https://huagongshe.com/reaction/1267512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzyl alcohol | HCID 122933 | — |
| Reactant | 2-(Chloromethyl)-1,1'-biphenyl | HCID 21972820 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(3,5-Bis-trifluoromethyl-benzyloxymethyl)-biphenyl | HCID 18546500 | 48.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06552088B2 |
|---|
| Source dataset | uspto-grants-2003_04 |
|---|
| ORD ID | ord-9989a3a214814205af9cba7f92f079fb |
|---|
| Source note | uspto-grants-2003_04 |
|---|