2-Bromopropane → HCID 67533734, compound

HRID 2358073Notes

Reaction equation

HRID 2358073 reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([C:13]([F:16])([F:15])[F:14])[C:8]=2[OH:17])[CH2:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+].[CH:24](Br)([CH3:26])[CH3:25]>C(#N)C>[CH:24]([N:1]1[CH2:6][CH2:5][CH:4]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([C:13]([F:15])([F:16])[F:14])[C:8]=2[OH:17])[CH2:3][CH2:2]1)([CH3:26])[CH3:25]

Participants

5

Reactant 3

HCID 63582-BromopropaneHCID 11430Potassium CarbonateHCID 57448052HCID 57448052, compound

Product 1

HCID 67533734HCID 67533734, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Preparation according to Example 1: 2-piperidin-4-yl-6-(trifluoromethyl)phenol (0.01 g, 0.04 mmol), acetonitrile (2 ml), potassium carbonate (0.01 g) and isopropyl bromide (0.01 ml). MS m/z (relative intensity, 70 eV) 287 (M+, 13), 272 (bp), 253 (13), 252 (44), 166 (12).

Workup

  1. customPreparation

Sources & evidence

ORD record
ord-c4f133aa0449480e9a5d79ee7ee90ade
Source dataset
uspto-grants-2010_07
Patent number
US07763639B2

Reaction notes

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