Ammonium formate → Methyl 4-hydroxyphenyllactate

HRID 1004198Notes

Reaction equation

HRID 1004198 reaction equation
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH:16]([OH:21])[C:17]([O:19][CH3:20])=[O:18])=[CH:11][CH:10]=1)C1C=CC=CC=1.C([O-])=O.[NH4+]>CO.[Pd]>[OH:21][CH:16]([CH2:15][C:12]1[CH:11]=[CH:10][C:9]([OH:8])=[CH:14][CH:13]=1)[C:17]([O:19][CH3:20])=[O:18]

Participants

5

Procedure

A solution of methyl 3-(4-benzyloxyphenyl)-2-hydroxypropanoate (c.f International Patent Appl., Publication No. WO 9101337) (5.72 g) in methanol (120 mL) was added to an ice cooled suspension of 10% Palladium charcoal (1.90 g) in methanol (30 mL) under a nitrogen atmosphere. Solid ammonium formate (6.4 g) was added and the mixture heated at reflux for 15 minutes, then allowed to cool to room temperature. The catalyst was removed by filtering the reaction mixture through diatomaceous earth and the solvent evaporated. The residue was suspended in dilute hydrochloric acid (2M, 100 mL) and extracted with ethyl acetate (2×400 mL). The combined ethyl acetate solutions were washed with water (400 mL), brine (400 mL), dried (MgSO4) and evaporated. The resulting gum was chromatographed on silica gel with 1.5% methanol in dichloromethane as eluent to afford the title compound, mp 42-43° C.

Workup

  1. temperaturecooled
  2. temperaturethe mixture heated
  3. temperatureat reflux for 15 minutes
  4. customThe catalyst was removed
  5. filtrationby filtering the reaction mixture through diatomaceous earth
  6. customthe solvent evaporated
  7. extractionextracted with ethyl acetate (2×400 mL)
  8. washThe combined ethyl acetate solutions were washed with water (400 mL), brine (400 mL)
  9. dry with materialdried (MgSO4)
  10. customevaporated
  11. customThe resulting gum was chromatographed on silica gel with 1.5% methanol in dichloromethane as eluent

Sources & evidence

ORD record
ord-32594abe0d544411b7967aa8e0b48df7
Source dataset
uspto-grants-2000_04
Patent number
US06048883

Reaction notes

Loading…