HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427610Generated: October 30, 2026
2-Methoxy-5-nitroaniline → Carbamic acid, (2-methoxy-5-nitrophenyl)-, phenylmethyl ester
https://huagongshe.com/reaction/427610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxy-5-nitroaniline | HCID 7447 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Carbamic acid, (2-methoxy-5-nitrophenyl)-, phenylmethyl ester | HCID 4935662 | 86% |
Reaction Steps
To a stirred solution of 2-methoxy-5-nitroaniline (5.0 g, 30 mmol) and potassium carbonate (12 g, 90 mmol) in tetrahydrofuran (200 mL) and water (100 mL) was added benzyl chloroformate (6.1 g, 36 mmol). After 12 h, the mixture was diluted with ethyl acetate (200 mL) and the layers were separated. The organic phase was washed twice with 1 N aqueous hydrochloric acid, once with saturated aqueous sodium chloride solution, twice with saturated aqueous sodium bicarbonate solution, twice with saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated in vacuo. The resulting solid was suspended in diethyl ether and after sonication, the solid was filtered, washed with diethyl ether, and dried in vacuo to give 7.8 g (86%) of the title compound as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06313122B1 |
|---|
| Source dataset | uspto-grants-2001_11 |
|---|
| ORD ID | ord-1e055435ee044e48a75ca3c72af4c6a7 |
|---|
| Source note | uspto-grants-2001_11 |
|---|