Sodium borohydride → (3,4-Dimethoxy-5-propylphenyl)methanol

HRID 476670Notes

Reaction equation

HRID 476670 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([CH2:13][CH2:14][CH3:15])[C:10]=1[O:11][CH3:12])[CH:6]=[O:7].[BH4-].[Na+]>CC(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:6][OH:7])[CH:8]=[C:9]([CH2:13][CH2:14][CH3:15])[C:10]=1[O:11][CH3:12]

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 198382273,4-Dimethoxy-5-propylbenzaldehyde

Product 1

HCID 19838159(3,4-Dimethoxy-5-propylphenyl)methanolYield 72%

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

A solution of 3,4-dimethoxy-5-propylbenzaldehyde (11 g) and sodium borohydride (2 g) in 2-propanol (100 ml) was stirred at room temperature for 2 hours. The mixture was quenched with 2N HCl (200 ml) and extracted with ethyl acetate. The organic phase was separated, washed with brine, dried over MgSO4, filtered and evaporated to leave a yellow oil which was purified by Kugelrohr bulb to bulb distillation at 1 mm Hg air bath temperature 150° to give the sub-title compound as a colorless oil (8 g).

Workup

  1. customThe mixture was quenched with 2N HCl (200 ml)
  2. extractionextracted with ethyl acetate
  3. customThe organic phase was separated
  4. washwashed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customevaporated
  8. customto leave a yellow oil which
  9. distillationwas purified by Kugelrohr bulb to bulb distillation at 1 mm Hg air bath temperature 150°

Sources & evidence

ORD record
ord-9ccc28077d144ca1bc0e1b85a8d32713
Source dataset
uspto-grants-1989_12
Patent number
US04885313

Reaction notes

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