HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 3-Chloro-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3,3-Dichloro-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one | HCID 20442347 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Chloro-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one | HCID 20442349 | — |
Reaction Steps
A mixture of 3.06 g of 3,3-dichloro-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one, 30 ml of glacial acetic acid, 2.2 g of anhydrous sodium acetate and 86 mg of 5% palladium on charcoal is hydrogenated at atmospheric pressure until the theoretical amount of hydrogen has been absorbed. The suspension is filtered through celite and the solids are washed with 5 ml of acetic acid. Concentration of the filtrate and treatment of the residue with 17 ml of water for 30 min. affords 3-chloro-5-methyl-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04477464 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-4f5a0568973b400cbad4db70243bd638 |
| Source note | uspto-grants-1984_10 |