Sodium Bicarbonate → HCID 17989217, compound

HRID 1869313Notes

Reaction equation

HRID 1869313 reaction equation
C([O:3][C:4](=O)[C:5]([C:24]([F:27])([F:26])[F:25])([O:19][Si:20]([CH3:23])([CH3:22])[CH3:21])[CH2:6][C:7]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[C:11]=1[O:17][CH3:18])([CH3:9])[CH3:8])C.[H-].[H-].[H-].[H-].[Li+].[Al+3].C([O-])(O)=O.[Na+]>C(OCC)C>[F:16][C:12]1[C:11]([O:17][CH3:18])=[C:10]([C:7]([CH3:8])([CH3:9])[CH2:6][C:5]([C:24]([F:26])([F:27])[F:25])([O:19][Si:20]([CH3:22])([CH3:23])[CH3:21])[CH2:4][OH:3])[CH:15]=[CH:14][CH:13]=1

Participants

5

Procedure

5.24 g (12.34 mmol) of 4-(3-fluoro-2-methoxyphenyl)-4-methyl-2-trifluoromethyl-2-trimethylsilyloxy-pentanoic acid ethyl ester is dissolved in 45 ml of diethyl ether and mixed at 0 to 5° C. in portions with 936.9 mg (24.69 mmol) of LiAlH4. After four and one-half hours of stirring at room temperature, the reaction mixture is carefully mixed with saturated NaHCO3 while being stirred in an ice bath, stirred for one hour under cold conditions and overnight at room temperature. After the conventional working-up, 4.11 g (87.1%) of a mixture that consists of the desired compound and the compound is obtained, in which the silyl ether has migrated. The mixture is incorporated in crude form into the next stage.

Workup

  1. stirringwhile being stirred in an ice bath
  2. stirringstirred for one hour under cold conditions and overnight at room temperature

Sources & evidence

ORD record
ord-f28124a3a13846d6914ee9ed329f99a9
Source dataset
uspto-grants-2009_12
Patent number
US07638515B2

Reaction notes

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