HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → benzyl N-(2-hydroxyethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | benzyl N-(2-hydroxyethyl)carbamate | HCID 280458 | 94.5% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To ethanolamine (9.0 ml, 149 mmol) in methylene chloride (100 ml) at 0° C. was added benzyl chlorformate (10.0 ml, 70 mmol). The mixture was stirred at 0° C. for 30 min, then at room temperature for 1 h, poured into ethyl acetate, washed with 2M HCl, saturated NaHCO3 solution, and brine, then dried over Na2SO4 and evaporated to provide 12.91 g (94%) of the desired compound as a white solid. 1H NMR (CDCl3, TMS) 7.47 (m,5H), 5.11 s,2H), 3.73 (m,2H), 3.38 (m,2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05059589 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-16ebb065b3f54bd6bf06620dc74a6728 |
| Source note | uspto-grants-1991_10 |