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Water → 2-[4-(4-Trifluoromethylpyridin-2-yloxy)-phenyl]-ethanol

HRID 339813
Notes
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Reaction equation

HRID 339813 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][OH:10])=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].F[C:18]1[CH:23]=[C:22]([C:24]([F:27])([F:26])[F:25])[CH:21]=[CH:20][N:19]=1.O>CS(C)=O>[F:25][C:24]([F:27])([F:26])[C:22]1[CH:21]=[CH:20][N:19]=[C:18]([O:1][C:2]2[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][OH:10])=[CH:4][CH:3]=2)[CH:23]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 10393TyrosolHCID 11430Potassium CarbonateHCID 111595142-Fluoro-4-(trifluoromethyl)pyridine

Product 1

HCID 581742462-[4-(4-Trifluoromethylpyridin-2-yloxy)-phenyl]-ethanolYield 75.4%

Reagents, catalysts & solvents 1

HCID 679
Dimethyl Sulfoxide
Solvent

Conditions

Temperature
25 °C

Procedure

2-(4-Hydroxyphenyl)ethanol (4.0 g, 29 mmol), K2CO3 (8.0 g, 58 mmol) and 2-fluoro-4-trifluoromethylpyridine (3.6 g, 22 mmol) were combined in DMSO (30 mL) and stirred at 25° C. for 20 h. The mixture was poured into H2O and extracted twice with Et2O. The combined Et2O extracts were washed with 1M NaOH, H2O, brine, and concentrated in vacuo to give 2-[4-(4-trifluoromethylpyridin-2-yloxy)-phenyl]-ethanol (4.7 g; 57%), mp 78-79° C.; EIMS m/z 283; 1H NMR (300 MHz, DMSO-d6) δ 8.38 (d, J=5.3 Hz, 1H), 7.0-7.5 (m, 8H), 4.67 (t, J=5.0 Hz, 2H), 2.74 (t, J=5.2 Hz, 2H).

Workup

  1. extractionextracted twice with Et2O
  2. washThe combined Et2O extracts were washed with 1M NaOH, H2O, brine
  3. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-657573fce8ea451f8a3083ec107e46d2
Source dataset
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08895568B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes