Tert-butyl 2-oxa-3-azabicyclo[2.2.1]hept-5-ene-3-carboxylate → 1,1-Dimethylethyl N-((1S,3R)-3-hydroxycyclopentyl)carbamate

HRID 931484Notes

Reaction equation

HRID 931484 reaction equation
[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[N:3]([C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9])[O:2]2>[Pd].CO>[OH:2][C@@H:1]1[CH2:6][CH2:5][C@H:4]([NH:3][C:8](=[O:9])[O:10][C:11]([CH3:13])([CH3:12])[CH3:14])[CH2:7]1

Participants

4

Conditions

Temperature
60 °C

Procedure

A mixture of tert-butyl 2-oxa-3-azabicyclo[2.2.1]hept-5-ene-3-carboxylate (8.0 g, 40.56 mmol, 1.00 equiv) and palladium on carbon (0.5 g) catalyst in methanol (100 mL) was stirred under an atmosphere of hydrogen atmosphere at 60° C. for 48 h. The reaction mixture was cooled to room temperature and the catalyst was removed by filtration. The catalyst was washed with 3×10 mL of MeOH. The combined filtrate and washings was concentrated under vacuum to give 6.5 g (80%) of tert-butyl N-[(1S,3R)-3-hydroxycyclopentyl]carbamate as a white solid. 1HNMR (400 MHz, D2O, ppm) δ 4.72 (1H, s), 4.55 (1H, s), 1.92-1.87 (3H, m), 1.76-1.60 (3H, m), 1.50 (9H, s).

Workup

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customthe catalyst was removed by filtration
  3. washThe catalyst was washed with 3×10 mL of MeOH
  4. concentrationThe combined filtrate and washings was concentrated under vacuum

Sources & evidence

ORD record
ord-4ec7db4e40b1433198f884d694fa84a2
Source dataset
uspto-grants-2016_03
Patent number
US09296732B2

Reaction notes

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