1-Butanol → HCID 10397079, compound

HRID 271969Notes

Reaction equation

HRID 271969 reaction equation
[CH2:1]([OH:5])[CH2:2][CH2:3][CH3:4].[C:6]([O:10][CH3:11])(=[O:9])C=C.C1N2[CH2:18][CH2:19]N(CC2)C1>>[CH3:11][O:10][C:6](=[O:9])[C:18](=[CH2:19])[CH:1]([OH:5])[CH2:2][CH2:3][CH3:4]

Participants

4

Procedure

A mixture of butanol (72.11 g, 1,000 mmol), methyl acrylate (129.14 g, 1,500 mmol) and DABCO (22.44 g, 200 mmol) is allowed to react at room temperature under N2 for 7 days. The reaction mixture is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent distills. The residue colorless liquid is dissolved in toluene (800 mL) and washed sequentially with 2 N HCl acid (250 mL), water (250 mL), saturated aq. sodium bicarbonate solution (120 mL) and water (150 mL). The toluene layer is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent distills to afford 3-hydroxy-2-methylenehexanoic acid methyl ester (96.7 g, yield: 61.1%) as a colorless liquid.

Workup

  1. customto react at room temperature under N2 for 7 days
  2. concentrationThe reaction mixture is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent
  3. distillationdistills
  4. dissolutionThe residue colorless liquid is dissolved in toluene (800 mL)
  5. washwashed sequentially with 2 N HCl acid (250 mL), water (250 mL), saturated aq. sodium bicarbonate solution (120 mL) and water (150 mL)
  6. concentrationThe toluene layer is concentrated on Rotavap under reduced pressure (20 mbar) until no further solvent
  7. distillationdistills

Sources & evidence

ORD record
ord-e5146dd307814c2f871203ea94b7319c
Source dataset
uspto-grants-2008_11
Patent number
US07452999B2

Reaction notes

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