Hydrochloric Acid → [2,6-Bis(trifluoromethyl)phenyl]methanol
Reaction equation
C[C:2]([O-:5])(C)C.[K+].[F:7][C:8]([F:20])([F:19])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:18])([F:17])[F:16])[CH:10]=1.[Li]CCCC.C=O.Cl>C1COCC1>[F:7][C:8]([F:19])([F:20])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([F:16])([F:17])[F:18])[C:10]=1[CH2:2][OH:5]Participants
Conditions
- Temperature
- -70 °C
Procedure
A mixture of 80 mL of THF and t-BuOK (7.0 g, 62.5 mmol) is added to a 250 mL four-neck flask equipped with a mechanical stirrer, a thermometer, a gas inlet tube and a 100 mL dropping funnel with a gas outlet tube. Cool down to −70° C. and 2,6-bis(trifluoromethyl)benzene (8.0 mL, 10.7 g, 50.0 mmol) is added dropwise and keep agitating ˜−70° C. for 30 min. Add n-BuLi (0.10 mol, 2.87 M in hexanes 35.0 mL, 100.0 mmol) dropwise over 30 min with agitation at ˜−70° C. for 60 min. Paraformaldehyde (6.0 g, 0.20 mol) is added and keep agitating ˜70° C. for 30 min, then gradually warm to room temperature for 3 h. Pour mixture into conc HCl (10 mL) and ice water (300 mL), and stir for 1 h. Extract with hexanes (3×50 mL). Wash the combined organic layers with 50 mL of brine, dry over anhydrous Na2SO4, filter and concentrate. The crude product is vacuum distilled (72-76° C. at 4-5 mm Hg) to give the desired compound (5 g).
Workup
- additionis added to a 250 mL four-neck flask
- customequipped with a mechanical stirrer
- stirringkeep agitating ˜70° C. for 30 min
- temperaturegradually warm to room temperature for 3 h
- stirringstir for 1 h
- extractionExtract with hexanes (3×50 mL)
- washWash the combined organic layers with 50 mL of brine
- dry with materialdry over anhydrous Na2SO4
- filtrationfilter
- concentrationconcentrate
- distillationdistilled (72-76° C. at 4-5 mm Hg)
Sources & evidence
- ORD record
- ord-da2d5e34cdd941ddb07bf7cd82e3089f
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07863310B2
Reaction notes
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