Potassium Carbonate → (4-Ethynyl-2-methyl-phenyl)-methanol

HRID 395185Notes

Reaction equation

HRID 395185 reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([C:8]#[C:9][Si](C)(C)C)[CH:5]=[CH:4][C:3]=1[CH2:14][O:15][Si](C)(C)C.C(=O)([O-])[O-].[K+].[K+]>CO>[C:8]([C:6]1[CH:5]=[CH:4][C:3]([CH2:14][OH:15])=[C:2]([CH3:1])[CH:7]=1)#[CH:9]

Participants

4

Procedure

Using General Procedure E; 2-methyl-4-trimethylsilanylethynyl-1-trimethylsilananyloxymethyl-benzene (Intermediate 135, 380.0 mg, 1.30 mmols) in methanol (10 mL) was treated with potassium carbonate (180.0 mg, 1.3 mmol) and stirred overnight at ambient temperature. The crude alkyne was purified by column chromatography (5-20% EtOAc-hexanes) to give 100.0 mg (34%) of the title compound.

Workup

  1. customThe crude alkyne was purified by column chromatography (5-20% EtOAc-hexanes)

Sources & evidence

ORD record
ord-839503e4aea1483b8df9ca603bfb0305
Source dataset
uspto-grants-2003_08
Patent number
US06603019B2

Reaction notes

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