HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 2-{[(Benzyloxy)carbonyl]amino}-2-methylpropyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | benzyl N-(1-hydroxy-2-methylpropan-2-yl)carbamate | HCID 12325553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{[(Benzyloxy)carbonyl]amino}-2-methylpropyl acetate | HCID 12325554 | — |
Reaction Steps
To a dichloromethane solution containing 2.52 g (0.011 mol) 2-carbobenzoxyamino-2-methyl-1-propanol and 1.17 g (0.015 mol) acetyl chloride was added dropwise with stirring 1.11 g (0.011 mol) triethylamine. The reaction was stirred at ambient temperature overnight and the dichloromethane was removed under reduced pressure. The triethylamine hydrochloride residue was triturated in anhydrous ether. Following filtration, the ether was removed under reduced pressure to afford 2.38 g (0.009 mol), 82%, crude 2-carbobenzoxyamino-2-methyl-1-propyl acetate as a pale yellow liquid, pmr (CDCl3) δ 7.2 (s, 5H), 5.4 (bs, 1H), 5.0 (s, 2H), 2.0 (s, 3H) and 1.2 (s, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04092420 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-684958aeacef44e1b4984cf93c183f7a |
| Source note | uspto-grants-1978_05 |