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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366359Generated: November 4, 2026

4-Nitrophenyl morpholin-4-ylcarbamate → HCID 23513714, compound

https://huagongshe.com/reaction/1366359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl morpholin-4-ylcarbamateHCID 20736284—
ReactantHCID 23513707HCID 23513707—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductHCID 23513714HCID 2351371482%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893057B2
Source datasetuspto-grants-2011_02
ORD IDord-e435601ec8004726bbdbff84fb9a27e6
Source noteuspto-grants-2011_02