HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borane → Tert-butyl N-(1-cyclohexyl-2-hydroxyethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | n-Boc-n-cyclohexylglycine | HCID 10563100 | — |
| Product | Tert-butyl N-(1-cyclohexyl-2-hydroxyethyl)carbamate | HCID 22037861 | 66.7% |
Reaction Steps
A solution of N-(t-butyloxycarbonyl)cyclohexylglycine (2.0 g, 7.77 mmol) in anhydrous THF (10 mL) was cooled to 0° C. Borane solution (1 M in THF, 15.5 mL, 15.5 mmol) was added slowly and the reaction mixture was warmed to room temperature and stirred for 2 hours. The reaction was quenched with MeOH (5 mL), volatiles were evaporated and the residue was partitioned between water and EtOAc. The organic layer was washed with saturated NaHCO3/water, brine, dried (sodium sulfate), and evaporated to give tert-butyl 1-cyclohexyl-2-hydroxyethylcarbamate 2a (1.26 g, 66.7%), MS (CI) m/z 144.20 (MH+-Boc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071200B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-3e4b73e3d39440cc833debd0e62e047a |
| Source note | uspto-grants-2006_07 |