HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxide → HCID 15617817, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxide | HCID 961 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 15617779 | HCID 15617779 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 15617817 | HCID 15617817 | — |
Reaction Steps
A mixture of 3,4-dichlorobenzoic acid, 2-isopropylhydrazide (0.98 g, 0.004 mole) and benzoyl chloride (0.56 g, 0.004 mole) is stirred overnight in 1.2 mL of ethylene dichloride and 6.5 mL of 10% soldium hydroxide. The organic phase is removed and the aqueous mixture is extracted with 25 mL of ethylene dichloride. The organic extracts are combined and concentrated to a yellow oil which is taken up in hot isopropyl alcohol. Cooling the alcohol solution causes precipitation of the title compound as a white crystalline product, which is collected by filtration and has a mp of 157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04814349 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-38e543949e3244f1bfc2218cb8e9ecbc |
| Source note | uspto-grants-1989_03 |