HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl succinimido carbonate → Benzyl (2r)-3-(4-cyanophenoxy)-2-hydroxypropylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | 4-{[(2R)-3-Amino-2-hydroxypropyl]oxy}benzonitrile | HCID 30072096 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl (2r)-3-(4-cyanophenoxy)-2-hydroxypropylcarbamate | HCID 91135093 | 100% |
Reaction Steps
A mixture of 4{[(2R)-3-amino-2-hydroxypropyl]oxy}benzonitrile (see step (ii) above; 3.4 g, 17.7 mmol), TEA (2.69 g, 26.6 mmol) and CHCl3 (20 mL) was cooled to 0° C. before N-(benzyloxycarbonyloxy)succinimide (4.86 g, 19.5 mol) in CHCl3 (15 mL) was added slowly. The mixture was allowed to reach rt, and was stirred at that temperature overnight. The solvent was evaporated to give a residue that was dissolved in DCM. This solution was washed with water and brine and then dried (Na2SO4). Evaporation of the solvent gave 5.79 g (100%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559162B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-9df57f2bfb3e467fbbe6b80865b95060 |
| Source note | uspto-grants-2003_05 |