tert-Butanol → [4-(4-Chloro-phenyl)-cyclohexyl]-carbamic acid tert-butyl ester

HRID 1048154Notes

Reaction equation

HRID 1048154 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:13][CH2:12][CH:11](C(O)=O)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C([N:19]([CH2:22]C)CC)C.P(N=[N+]=[N-])(=O)(OC1C=CC=CC=1)[O:25]C1C=CC=CC=1.[C:43]([OH:47])([CH3:46])([CH3:45])[CH3:44]>CCOC(C)=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:9][CH2:10][CH:11]([NH:19][C:22](=[O:25])[O:47][C:43]([CH3:46])([CH3:45])[CH3:44])[CH2:12][CH2:13]2)=[CH:6][CH:7]=1

Participants

6

Procedure

To a solution of 4-(4-chlorophenyl)cyclohexanecarboxylic acid (1.01 g, 4.231 mmol) and triethylamine (0.5897 ml, 4.231 mmol) in tert-butanol (22 ml) was added diphenyl phosphorazidate (0.9147 ml, 4.231 mmol), and the reaction was heated to reflux for 16 hours. The reaction was diluted with EtOAc and washed with 1M hydrochloric acid, saturated sodium bicarbonate, and saturated sodium chloride. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated. The crude material was on a Biotage SP1 system eluting with a linear gradient of 5-50% EtOAc in hexanes to yield 760 mg of the title compound (57% yield).

Workup

  1. temperaturethe reaction was heated
  2. temperatureto reflux for 16 hours
  3. washwashed with 1M hydrochloric acid, saturated sodium bicarbonate, and saturated sodium chloride
  4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. washeluting with a linear gradient of 5-50% EtOAc in hexanes

Sources & evidence

ORD record
ord-06f978a8581b4161a9db09b1202f4c5d
Source dataset
uspto-grants-2013_10
Patent number
US08569522B2

Reaction notes

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