Sodium Sulfate → 2-(Benzyloxy)propan-1-ol

HRID 537647Notes

Reaction equation

HRID 537647 reaction equation
[CH2:1]([O:8][C:9]([CH3:16])(O)[C:10](OCC)=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].S([O-])([O-])(=O)=O.[Na+].[Na+]>O1CCCC1>[CH2:1]([O:8][CH:9]([CH3:16])[CH2:10][OH:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Conditions

Temperature
60 °C

Procedure

A solution of ethyl 2-benzyloxylactate (9.5 g, 45.6 mmole) in anhydrous tetrahydrofuran (30 mL) was added dropwise during 30 minutes to a stirred solution of lithium aluminum hydride (1.06 g, 28 mmole) in anhydrous tetrahydrofuran (56 mL) at room temperature under argon atmosphere. Next, the mixture was stirred for 3 hours at 60° C. After cooling to 30° C., freshly prepared saturated solution of sodium sulfate (10 mL) was slowly added. The mixture was filtered and the solvent was distilled under reduced pressure. The residue was dissolved in dichloromethane (100 mL) and the solution was dried with anhydrous magnesium sulfate. The solvent then was distilled under reduced pressure. The residue was subjected to fractional vacuum distillation giving 6.2 g of colorless liquid product. NMR (d6-DMSO): 1.90 ppm (d, —CH3, 3H), 3.20-3.50 ppm (bm, —CH— and —CH2—, 3H), 4.53 ppm (s, —CH2—, 2H), 4.63 ppm (t, —OH, 1H), 7.33 ppm (m, 5H).

Workup

  1. temperatureAfter cooling to 30° C.
  2. filtrationThe mixture was filtered
  3. distillationthe solvent was distilled under reduced pressure
  4. dissolutionThe residue was dissolved in dichloromethane (100 mL)
  5. dry with materialthe solution was dried with anhydrous magnesium sulfate
  6. distillationThe solvent then was distilled under reduced pressure
  7. distillationThe residue was subjected to fractional vacuum distillation

Sources & evidence

ORD record
ord-de56e16912314998a201687a5144cf34
Source dataset
uspto-grants-2014_10
Patent number
US08865149B2

Reaction notes

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