HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroveratraldehyde → N-(2-chloro-3,4-dimethoxybenzylideneamino)-N'-hydroxy-N''-phenylguanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroveratraldehyde | HCID 79445 | — |
| Reactant | HCID 178427661 | HCID 178427661 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-chloro-3,4-dimethoxybenzylideneamino)-N'-hydroxy-N''-phenylguanidine | HCID 86590910 | — |
Reaction Steps
0.22 g (1.1 mmol) 2-chloro-3,4 dimethoxybenzaldehyde and 0.34 g (1 mmol) N-hydroxy-N′-phenylaminoguanidine tosylate was mixed in 7 ml methanol. The reaction mixture was refluxed for 80 min after which it was cooled down, to room temperature. The solvent was evaporated and 10 ml acetonitile was added and the solution was stirred for 1 h. The precipitate formed was filtered, washed with ether and subseqently dried. The yield of title compound 2 was 0.40 g (77%) as a crystalline solid M.p. 167–169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153881B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-bf477626a78644a384a8cc8ca00661d9 |
| Source note | uspto-grants-2006_12 |