HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenol → ethyl N-[2-(4-nitrophenoxy)ethyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-chloroethylcarbamate | HCID 80621 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | ethyl N-[2-(4-nitrophenoxy)ethyl]carbamate | HCID 15662591 | — |
Reaction Steps
To sodium hydride (1.35 g, 56.2 mmol), prewashed in hexane, in 30 ml of DMF is added 4-nitrophenol in 5 ml of DMF at 15°. After anion formation is complete, ethyl N-chloroethylcarbamate (7.12 g, 47.0 mmol) is slowly added. The slurry is heated to 85° and stirred for 17 hours, after which the reaction is cooled to RT, poured into ice water and ether, and extracted with ether. The combined organic layers are washed with 10% sodium hydroxide, with water and with brine, dried and filtered and the solvent is removed by rotoevaporation to give ethyl N-[2-(4-nitrophenoxy)ethyl]carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04968829 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-204d540688964e2ea8d87a6feb8ab354 |
| Source note | uspto-grants-1990_11 |