HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzaldehyde → HCID 53834340, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | HCID 21824527 | HCID 21824527 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53834340 | HCID 53834340 | 74% |
Reaction Steps
An amount of 1.4 g. of 6-chloro-4-(1-methylhydrazino)-1H-2,3-benzoxazine is dissolved in 70 ml. of ethanol by heating at 50° C, then 1.12 g. of p-nitro-benzaldehyde are added. The solution is stirred, then allowed to stand for 2 hours. The formed crystals are collected by filtering and recrystallized from 500 ml. of benzene. An amount of 1.7 g. (74%) of 6-chloro-4-[1-methyl-2-(4-nitro-benzylidene)-hydrazino]-1H-2,3-benzoxazine are obtained; m.p. 251° C with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005082 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-199fa85625d9407bb67a2e5a3801f4d2 |
| Source note | uspto-grants-1977_01 |