HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Aminocyclohexanecarboxylic acid → 1-(Cbz-amino)cyclohexanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Aminocyclohexanecarboxylic acid | HCID 1366 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(Cbz-amino)cyclohexanecarboxylic acid | HCID 11357886 | 89.1% |
Reaction Steps
To a solution of l-aminocyclohexane-1-carboxylic acid (10.0 g, 70.0 mmol) in a 1M NaOH solution (100 mL) was added benzyl chloroformate (12.0 ml, 84.0 mmol). The reaction mixture was stirred for 2 h while maintaining pH 9 by addition of a 1M NaOH solution as necessary. The resulting solution was washed with Et2O (2×100 mL), then the aqueous layer was adjusted to pH 0 with a conc. HCl solution and the solution was extracted with EtOAc (3×150 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to yield 1-(benzyloxycarbonylamino)cyclohexane-1-carboxylic acid (17.3 g, 89%): TLC (25% EtOAc/hex) Rf0.07.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-96e8f18f2acb48c4a45d10eda0248a35 |
| Source note | uspto-grants-2002_03 |