Methanol → HCID 21904646, compound

HRID 1717466Notes

Reaction equation

HRID 1717466 reaction equation
C[O:2][C:3](=[O:18])[CH:4]([C:7]1[CH:12]=[C:11]([O:13][CH:14]([F:16])[F:15])[CH:10]=[C:9]([Cl:17])[CH:8]=1)[CH:5]=[O:6].CO.[BH4-].[Na+]>C1COCC1.C(OCC)(=O)C.O>[Cl:17][C:9]1[CH:8]=[C:7]([CH:12]=[C:11]([O:13][CH:14]([F:15])[F:16])[CH:10]=1)[CH:4]([CH2:5][OH:6])[C:3]([OH:18])=[O:2]

Participants

7

Procedure

α-Formyl(3-chloro-5-difluoromethoxyphenyl)acetic acid methyl ester (400 mg, 1.4 mmol; see step (vii) above) was dissolved in THF:methanol (50 mL, 9:1). Sodium borohydride was added and the mixture was stirred at ambient temperature for 30 minutes. Water was added and the mixture was concentrated to produce an aqueous suspension, which was taken up in ethyl acetate and water. The phases were separated and the organic phase washed with sodium chloride (15% in water), dried over sodium-sulphate, filtered and concentrated at reduced pressure. The residue was dissolved in methanol (30 mL) and hydrolyzed with sodium hydroxide (1 mL, 10 M) at ambient temperature for 10 minutes. Extractive work up gave 180 mg, 0.68 mmol (yield: 48%) of the sub-title compound.

Workup

  1. concentrationthe mixture was concentrated
  2. customto produce an aqueous suspension, which
  3. customThe phases were separated
  4. washthe organic phase washed with sodium chloride (15% in water)
  5. dry with materialdried over sodium-sulphate
  6. filtrationfiltered
  7. concentrationconcentrated at reduced pressure
  8. dissolutionThe residue was dissolved in methanol (30 mL) and hydrolyzed with sodium hydroxide (1 mL, 10 M) at ambient temperature for 10 minutes

Sources & evidence

ORD record
ord-f61c2de20967440caea4f5ec59013fa4
Source dataset
uspto-grants-2010_09
Patent number
US07803954B2

Reaction notes

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