HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 23467138, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 23467157 | HCID 23467157 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23467138 | HCID 23467138 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 0.5 g of 2-(2-aminopropyl)-5-pyridinol hydrochloride, 0.85 g of benzoyl chloride, 10 ml of methylene chloride and 10 ml of saturated aqueous sodium bicarbonate is stirred at room temperature for 1 hour. The organic phase is separated, dried evaporated and the residue recrystallized from diethyl ether to give the dibenzoyl-2-(2-aminopropyl)-5-pyridinol melting at 110°-112°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260619 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-b9b14f1674b04d2c8283dd06d2a21eef |
| Source note | uspto-grants-1981_04 |