HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → Ethyl(3-{[(benzyloxy)carbonyl]amino}phenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 3-aminophenylacetate | HCID 13054266 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl(3-{[(benzyloxy)carbonyl]amino}phenyl)acetate | HCID 57907493 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of methyl (3-aminophenyl)acetate (25 g, 140 mmol) in 250 mL anhydrous DCM was added DIEA (28.5 mL, 155 mmol) and the resulting solution cooled to 0° C. and set under nitrogen atmosphere. To this cooled solution was then added benzyl chloroformate (21.1 mL, 148 mmol) and the resulting mixture stirred overnight allowing to warm to room temperature. The reaction was washed with 1 M HCl, water, and then brine. The organic layer was dried over sodium sulfate, filtered and concentrated under vacuum. No further purification was necessary and the material (44 g, 99%) was used as is for the next step reaction. LC-MS: m/z (ES) 314 (MH)+, 336 (MNa)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653260B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-99c5c4fb42c34c63ba28b8078c31b16d |
| Source note | uspto-grants-2014_02 |