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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288271Generated: October 31, 2026

Water → 2-(2-Allyloxyphenyl)-4-amino-5-nitrosopyrimid-6-one

https://huagongshe.com/reaction/1288271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodiumHCID 5360545—
ReactantEthyl 2-cyano-2-(hydroxyimino)acetateHCID 6399078—
ReactantHCID 22462384HCID 22462384—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product2-(2-Allyloxyphenyl)-4-amino-5-nitrosopyrimid-6-oneHCID 13635461555.9%

Reaction Steps

2-Allyloxybenzamidine hydrochloride (10.2 g.) was added to a solution of sodium (4.6 g.) in anhydrous methanol (200 ml.) with stirring, followed by ethyl α-oximinocyanoacetate (7.6 g.), and the mixture was stirred under reflux for 6 hours. The hot mixture was poured into water (500 ml.) and acidified with glacial acetic acid. The blue solid was filtered off, washed with water and recrystallised from 50% aqueous acetic acid to give 2-(2-allyloxyphenyl)-4-amino-5-nitrosopyrimid-6-one (7.3 g.), m.p. 217°-220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987160
Source datasetuspto-grants-1976_10
ORD IDord-b1c2585a22d04eddb25559fb155bd831
Source noteuspto-grants-1976_10