HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 14579395, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14579478 | HCID 14579478 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14579395 | HCID 14579395 | 84.5% |
Reaction Steps
A mixture of 4.64 g of (±)-4-(2-amino-1-methylethyl)phenol hydrobromide, 100 ml of ethyl acetate, 6.92 g of potassium carbonate, 40 ml of water and 3.75 g of benzyloxycarbonyl chloride is stirred at room temperature overnight. After the reaction, the ethyl acetate layer is separated therefrom, washed, dried, and then evaporated under reduced pressure to remove the solvent. 4.82 g of (±)-4-(2-benzyloxycarbonylamino-1-methylethyl)phenol are obtained as pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04866196 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-65d215a4ce064f279b0a1a1aa416cc97 |
| Source note | uspto-grants-1989_09 |