Acetic Anhydride → Benzyl propionate

HRID 487814Notes

Reaction equation

HRID 487814 reaction equation
[CH2:1]([O:8][C:9](=[O:20])[CH:10](N)[CH2:11]C1C=CC=C(O)C=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC(=O)C)(=O)C.C(=O)([O-])[O-].[Na+].[Na+]>O>[CH2:1]([O:8][C:9](=[O:20])[CH2:10][CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Reactant 3

HCID 7918Acetic Anhydride2×HCID 10340Sodium CarbonateHCID 14888692Benzyl 2-amino-3-(3-hydroxyphenyl)propanoate

Product 1

HCID 31219Benzyl propionate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A suspension of 3.72 g (0.032 mol) of rac.-2-amino-3-(3-hydroxyphenyl)propanoic acid benzyl ester in 400 mL of ice cold dichloromethane was treated dropwise with 1.9 mL (0.020 mol) of acetic anhydride. Upon completion of the addition, a solution of 3.70 g of sodium carbonate in 30 mL of water was added simultaneously with an additional 1.9 mL of acetic anhydride. After 1 hour, the layers were separated and the organic layer was washed with water. The combined aqueous layers were extracted with dichloromethane and the combined is extracts were washed with brine and dried over magnesium sulfate. Filtration and concentration afforded a residue which was chromatographed on a Waters Prep 500 liquid chromatograph fitted with two silica gel cartridges, eluting with 20% ethyl acetate-hexane to give 8.49 g (84%) of rac.-2-acetamido-3-hydroxyphenyl)propanoic acid benzyl ester as a thick oil.

Workup

  1. additionUpon completion of the addition
  2. customthe layers were separated
  3. washthe organic layer was washed with water
  4. extractionThe combined aqueous layers were extracted with dichloromethane
  5. washwere washed with brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationFiltration and concentration
  8. customafforded a residue which
  9. customwas chromatographed on a Waters Prep 500 liquid chromatograph
  10. customfitted with two silica gel cartridges
  11. washeluting with 20% ethyl acetate-hexane

Sources & evidence

ORD record
ord-c78f59d4d17647dfb6dbd82ba1971fae
Source dataset
uspto-grants-1994_03
Patent number
US05296608

Reaction notes

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