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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918247Generated: October 31, 2026

Ethanol → HCID 13207879, compound

https://huagongshe.com/reaction/918247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCarbamic acid, ethyl esterHCID 5641—
ReactantHCID 21521530HCID 21521530—
CatalystZincchlorideHCID 3007855—
SolventChloroformHCID 6212—
ProductHCID 13207879HCID 13207879—

Reaction Steps

A mixture of 3.9 g of 2-(1-adamantylmethyl-amino)-5-nitrobenzophenone, 6.4 g of ethyl carbamate and 0.45 g of anhydrous zinc chloride was heated at 170°- 180°C for 1 hour, and then, distillating off the produced ethanol, heating was continued at that temperature for additional 1 hour. After cooling, chloroform was added thereto and insoluble material was filtered off. The chloroform layer was washed with water and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residual oil was chromatographed on silica gel using chloroform as eluting solvent to give 1-(1-adamantylmethyl)-4-phenyl-6-nitro-2(1H)-quinazolinone, m.p. 230°- 233°C, following recrystallization from a mixture of ethanol and chloroform.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03970654
Source datasetuspto-grants-1976_07
ORD IDord-f3fc40424b9344b498fab6c9f66a366d
Source noteuspto-grants-1976_07