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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353435Generated: October 30, 2026

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

https://huagongshe.com/reaction/353435

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 numberUS06753329B2
Source datasetuspto-grants-2004_06
ORD IDord-44876ec5d0b347e1b550d787396a8a34
Source noteuspto-grants-2004_06