tert-Butanol → N-1-Boc-Amino-3-cyclopentene
Reaction equation
[CH:1]1(C(O)=O)[CH2:5][CH:4]=[CH:3][CH2:2]1.C([N:11]([CH2:14]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:23])C=CC=CC=1.[C:33]([OH:37])([CH3:36])([CH3:35])[CH3:34]>>[CH:1]1([NH:11][C:14](=[O:23])[O:37][C:33]([CH3:36])([CH3:35])[CH3:34])[CH2:2][CH:3]=[CH:4][CH2:5]1Participants
Procedure
To a solution of 3-cyclopentene-1-carboxylic acid (J.-P. Depres and A. E. Greene, J. Org. Chem. 1984, 49:928-931; 29.71 g, 0.261 mole), triethylamine (36.4 mL) in t-butanol (1 L) was added diphenylphosphoryl azide, Aldrich, 97%, 74.0 g, 0.261 mmole). The solution was maintained at 60--C. for 4 hours. Cuprous chloride (1.3 g) was added and stirring continued at ambient temperature for 18 hours. Volatiles were evaporated and the residue was dissolved in methylene chloride (1250 mL) and washed with 10 % aqueous sodium carbonate (2×250 mL) and dried (magnesium sulfate). Volatiles were evaporated and the residue was chromatographed on a silica gel column. Title compound was eluted with chloroform as white crystals, from hexanes (22.63 g, 47%), m.p. 68-70° C.
Workup
- temperatureThe solution was maintained at 60
- waitcontinued at ambient temperature for 18 hours
- customVolatiles were evaporated
- dissolutionthe residue was dissolved in methylene chloride (1250 mL)
- washwashed with 10 % aqueous sodium carbonate (2×250 mL)
- dry with materialdried (magnesium sulfate)
- customVolatiles were evaporated
- customthe residue was chromatographed on a silica gel column
- washTitle compound was eluted with chloroform as white crystals, from hexanes (22.63 g, 47%), m.p. 68-70° C.
Sources & evidence
- ORD record
- ord-7d52b3919c5145259226aa4612df7ffd
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998398
Reaction notes
Loading…