HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → Ethyl (4-bromo-2-cyanophenyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Amino-5-bromobenzonitrile | HCID 429740 | — |
| Product | Ethyl (4-bromo-2-cyanophenyl)carbamate | HCID 18367857 | 68% |
Reaction Steps
A suspension of 2-amino-5-bromobenzonitrile (58.5 g, 297 mmol) in ethyl chloroformate (141 mL, 1.48 mol) was heated at reflux for 5 h. The excess ethyl chloroformate (99 mL) was distilled off and toluene (96 mL) was added. Slow addition of cyclohexane (228 mL) induced crystallization. The resulting solid was collected by filtration and rinsed with cyclohexane. Drying in vacuo afforded the title compound (54.3 g, 68%) as an orange solid. MS: m/e=267.1/269.2 [M—H−].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507728B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-c226dfd0b3a249e6993d3cfb1ff6271d |
| Source note | uspto-grants-2009_03 |