Glycolic Acid → Benzyl 2-hydroxyacetate

HRID 849741Notes

Reaction equation

HRID 849741 reaction equation
[H-].[Na+].[C:3]([OH:7])(=[O:6])[CH2:4][OH:5].[CH2:8](Br)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>C1COCC1>[C:3]([O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:6])[CH2:4][OH:5]

Participants

5

Conditions

Temperature
25 °C

Procedure

Alternatively, to a cold (0° C. ) suspension of NaH (3.8 g of a 60% weight dispersion in mineral oil, 95.0 mmol) in THF (50 mL) was added a solution of glycolic acid (7.2 g, 95 mmol) in THF (50 mL) dropwise via cannula. The resulting solution was warmed to 25° C. and concentrated in vacuo. The resulting salt was suspended in DMF (100 mL) and treated with KI (1.57 g, 0.1 eq) and benzyl bromide (12.3 mL, 1.1 eq). The mixture was heated at 100° C. for 23 hours under argon and the DMF was evaporated. The residue was dissolved in ether and washed with water, saturated Na2S2O3, and brine, and dried over MgSO4. Distillation afforded benzyl glycolate (8.5 g, 54%) as a colorless oil, b.p. 85-87° C. (0.5 Torr).

Workup

  1. concentrationconcentrated in vacuo
  2. temperatureThe mixture was heated at 100° C. for 23 hours under argon
  3. customthe DMF was evaporated
  4. dissolutionThe residue was dissolved in ether
  5. washwashed with water, saturated Na2S2O3, and brine
  6. dry with materialdried over MgSO4
  7. distillationDistillation

Sources & evidence

ORD record
ord-200a54ad53424f6a99598112b15849a3
Source dataset
uspto-grants-2000_01
Patent number
US06013792

Reaction notes

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