HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → benzyl N-(1-hydroxy-2-methylpropan-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-2-methyl-1-propanol | HCID 11807 | — |
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl N-(1-hydroxy-2-methylpropan-2-yl)carbamate | HCID 12325553 | 100% |
Reaction Steps
A solution of 2-amino-2-methylpropan-1-ol (1.0 g, 11.2 mmol), triethylamine (1.7 mL, 12.2 mmol) and N-(benzyloxycarbonyloxy)-succinimide (3.1 g, 12.4 mmol) in THF (100 mL) at 0° C. were reacted for 0.5 hours then at room temperature for an additional hour. The reaction was concentrated and extracted with ethyl acetate (100 mL). The organic extract was washed sequentially with water, brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel, eluting with a gradient of ethyl acetate in dichloromethane (0-20%) to give the title compound as a colorless oil (2.5 g, quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910595B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-142e24590ca24defab85e952d975db2d |
| Source note | uspto-grants-2011_03 |