HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-Allyloxyphenyl)-4-amino-5-nitrosopyrimid-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl 2-cyano-2-(hydroxyimino)acetate | HCID 6399078 | — |
| Reactant | HCID 22462384 | HCID 22462384 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-Allyloxyphenyl)-4-amino-5-nitrosopyrimid-6-one | HCID 136354615 | 55.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987160 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-b1c2585a22d04eddb25559fb155bd831 |
| Source note | uspto-grants-1976_10 |