1,3-Propanediol → HCID 59792474, compound

HRID 1645604Notes

Reaction equation

HRID 1645604 reaction equation
[C:1]([O:9][CH2:10][C:11](=[O:14])[CH2:12][CH3:13])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:15](O)[CH2:16][CH2:17][OH:18].C(OCC)(OCC)OCC.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>C(OCC)C.C(OCC)(=O)C>[C:1]([O:9][CH2:10][C:11]1([CH2:12][CH3:13])[O:18][CH2:17][CH2:16][CH2:15][O:14]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

7

Procedure

A mixture of 2-oxobutyl benzoate (5 g, 26 mmol), 1,3-propanediol (5.94 g, 78 mmol), triethyl orthoformate (3.85 g, 26 mmol) and p-toluenesulfonic acid monohydrate (448 mg, 2.36 mmol) was stirred at room temperature for 3 hours and 30 minutes. To the reaction mixture, ethyl acetate and diethyl ether were added and the mixture was washed with water and a saturated saline solution. The organic layer was dried over sodium sulfate and filtrated. The filtrate was concentrated under reduced pressure. The residue was dissolved in heptane/ethyl acetate (12/1) and subjected to NH silica gel column chromatography (elution solvent: n-heptane/ethyl acetate=12/1) to obtain the title compound (4.33 g, 65.5%) as a colorless viscous oil.

Workup

  1. washthe mixture was washed with water
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. filtrationfiltrated
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. dissolutionThe residue was dissolved in heptane/ethyl acetate (12/1)
  6. washsubjected to NH silica gel column chromatography (elution solvent: n-heptane/ethyl acetate=12/1)

Sources & evidence

ORD record
ord-25dd7fd53fe849d4b5a0ac20da4877dd
Source dataset
uspto-grants-2012_02
Patent number
US08124780B2

Reaction notes

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