HCID 178526628, compound → HCID 178507586, compound

HRID 2077715Notes

Reaction equation

HRID 2077715 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C@H:10]2[CH2:13][C@H:12]([OH:14])[CH2:11]2)=[CH:6][CH:5]=1)([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([C@H:10]2[CH2:11][C@H:12]([OH:14])[CH2:13]2)=[CH:8][CH:9]=1

Participants

4

Procedure

To a stirred solution of trans-3-(4-nitrophenyl)cyclobutanol (step 3, 1.0 g, 4.9 mmol) in methanol (20 mL) was added 10% Pd—C (50 mg). The mixture was stirred at room temperature under hydrogen atmosphere for 2.5 h. The palladium catalyst was removed by filtration and washed with methanol (100 mL) and ethyl acetate (100 mL). The filtrate was concentrated under reduced pressure to afford 0.9 g (quant.) of the title compound as pale yellow solids:

Workup

  1. customThe palladium catalyst was removed by filtration
  2. washwashed with methanol (100 mL) and ethyl acetate (100 mL)
  3. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-d418476c7d624d5b803f184cd925b761
Source dataset
uspto-grants-2011_04
Patent number
US07928119B2

Reaction notes

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