HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → N-(2-methylbenzyloxycarbonyl)-tyrosinol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tyrosinol | HCID 151247 | — |
| Reactant | 2-Methylbenzyloxycarbonyl chloride | HCID 13292930 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(2-methylbenzyloxycarbonyl)-tyrosinol | HCID 53904979 | 72.9% |
Reaction Steps
In a mixture of 10 ml of water and 20 ml of ethyl acetate, 1.6 g of tyrosinol was dissolved. To the solution were added dropwise 2 g of 2-methylbenzyloxycarbonyl choride and 10 ml of an aqueous solution containing 1.3 g of sodium carbonate alternately with stirring while cooling with ice. After stirring for two hours at room temperature, the ethyl acetate layer was collected and washed with 5% hydrochloric acid and then with water. The layer was dried and concentrated to dryness. The residue was crystallized from ethyl acetate-petroleum either to give 2.2 g of N-(2-methylbenzyloxycarbonyl)-tyrosinol with a mp. 78°-81° C in a yield of 70%. Analysis, calculated for C18H21O4N C 68.55, H 6.72, N 4.44, found C 68.88, H 6.84, N 4.42.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04097608 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-d3cef8fbe5ee4015892ec82d5269c328 |
| Source note | uspto-grants-1978_06 |