HuagongsheHuagongshe Chemistry Print Report · For research reference only
Retinoyl chloride → Retinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Retinoyl chloride | HCID 10881705 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Retinamide | HCID 5370221 | 99% |
Reaction Steps
10 g (0.031 mole) of retinoic acid chloride as prepared according to the procedure described in Example 2 was added to the mixture of 300 ml of ammonia water (35%) and 100 ml of tetrahydrofuran and then stirred at room temperature for 20 hours. The reaction solution was distilled under reduced pressure and then concentrated. The residue was extracted with methylene chloride. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, filtered and then distilled under reduced pressure to obtain 9.43 g (Yield 99%) of the desired retinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06316644B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-6572553c177743bea7be0af2dd8a8236 |
| Source note | uspto-grants-2001_11 |