HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Benzyl ((2R)-1-hydroxypropan-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (R)-(-)-2-Amino-1-propanol | HCID 80308 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl ((2R)-1-hydroxypropan-2-yl)carbamate | HCID 6951254 | 98.2% |
Reaction Steps
11.42 g of benzyloxycarbonyl chloride were added dropwise to a mixture of 5.00 g of D-alaninol, 18.49 g of potassium carbonate, 15 ml of ethyl acetate and 15 ml of water, and the mixture was stirred at room temperature for 1.5 hours. At the end of this time, the ethyl acetate layer was separated, and the aqueous layer was extracted with ethyl acetate. The ethyl acetate layer and the extract were combined, dried over anhydrous sodium sulfate and then concentrated by evaporation under reduced pressure. The crude crystals which precipitated were collected by filtration and washed with hexane, to give 13.68 g of the title compound, melting at 78° C. to 80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05578620 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-9b3adef179e94f43ae9e04bf017ebfae |
| Source note | uspto-grants-1996_11 |