Acetic Acid → 2-Methyl-5-(4-(2-nitro-ethyl)-benzyl)-furan

HRID 640194Notes

Reaction equation

HRID 640194 reaction equation
[CH3:1][C:2]1[O:3][C:4]([CH2:7][C:8]2[CH:13]=[CH:12][C:11](/[CH:14]=[CH:15]/[N+:16]([O-:18])=[O:17])=[CH:10][CH:9]=2)=[CH:5][CH:6]=1.C(O)(=O)C.CS(C)=O.[BH4-].[Na+]>O>[CH3:1][C:2]1[O:3][C:4]([CH2:7][C:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][N+:16]([O-:18])=[O:17])=[CH:10][CH:9]=2)=[CH:5][CH:6]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 679Dimethyl SulfoxideHCID 4311764Sodium borohydrideHCID 592554362-Methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furan

Product 1

HCID 592555272-Methyl-5-(4-(2-nitro-ethyl)-benzyl)-furanYield 77%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a mixture of 2-methyl-5-(4-((E)-2-nitro-vinyl)-benzyl)-furan (120 mg) described in Manufacturing Example 46-1-4, acetic acid (0.2 mL) and dimethyl sulfoxide (3.4 mL) was added sodium borohydride (29 mg, 0.77 mmol) at room temperature while cooling appropriately, which was stirred for 20 minutes at room temperature. Water was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue was purified by neutral silica gel column chromatography (ethyl acetate:heptane=1:5) to obtain the title compound (90 mg, 77%).

Workup

  1. temperaturewhile cooling appropriately
  2. extractionwas then extracted with ethyl acetate
  3. washThe organic layer was washed with saturated aqueous sodium chloride
  4. concentrationwas concentrated under a reduced pressure
  5. customThe residue was purified by neutral silica gel column chromatography (ethyl acetate:heptane=1:5)

Sources & evidence

ORD record
ord-c2b2ba30ed444ec98e3d7e4b6c223f27
Source dataset
uspto-grants-2010_04
Patent number
US07691882B2

Reaction notes

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