HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrophenyl morpholin-4-ylcarbamate → HCID 23513714, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrophenyl morpholin-4-ylcarbamate | HCID 20736284 | — |
| Reactant | HCID 23513707 | HCID 23513707 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 23513714 | HCID 23513714 | 82% |
Reaction Steps
To a suspension of 4-amino-2-[4-(2-chloroethoxy)benzoyl]indan-1,3-dione (36 g, 105 mmol) in CH3CN (600 mL) was added morpholin-4-ylcarbamic acid 4-nitrophenyl ester (40 g, 120 mmol) followed by 4-dimethylaminopyridine (640 mg, 5.2 mmol). The reaction was heated at reflux for 4 hours then cooled to room temp. and stirred overnight. The bright yellow solid is collected by filtration, rinsed with Et2O and dried under vacuum to give the desired semicarbazide (40.5 g, 82% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06753329B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-44876ec5d0b347e1b550d787396a8a34 |
| Source note | uspto-grants-2004_06 |