HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[(4-chlorophenyl)methylideneamino]-4-methylbenzenesulfonamide → 4-Chlorobenzaldehyde tosyl hydrazone sodium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[(4-chlorophenyl)methylideneamino]-4-methylbenzenesulfonamide | HCID 333935 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Sodium | HCID 5360545 | — |
| Product | 4-Chlorobenzaldehyde tosyl hydrazone sodium salt | HCID 86638403 | 187.8% |
Reaction Steps
A 1 M sodium methoxyde solution was prepared by adding sodium (423 mg, 18.39 mmol) to anhydrous methanol (19 ml) with external cooling. Once all of the metal was dissolved, 4-chlorobenzaldehyde tosyl hydrazone (5.39 g, 17.51 mmol) was added and the mixture was stirred until the solid was dissolved. After stirring for a further 15 min at room temperature the methanol was removed under reduced pressure at room temperature. 5.73 g of 4-chlorobenzaldehyde tosyl hydrazone sodium salt was obtained in the form of a white powder (99% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08618023B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-e04e3be6279d4fd3afe9a8ad36ca1770 |
| Source note | uspto-grants-2013_12 |