HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963483Generated: October 30, 2026
Acetic Anhydride → HCID 135829355, compound
https://huagongshe.com/reaction/963483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178516818 | HCID 178516818 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 135829355 | HCID 135829355 | — |
Reaction Steps
To a suspension of 5-cyclohexy-2,3-dihydro-1H-1,4-benzodiazepin-2-one-4-oxide (0.70 g) in chloroform (10 ml) was added acetic anhydride (3.7 ml) at ambient temperature and the mixture was heated for 4 hours at 70° C. After cooling, the mixture was concentrated in vacuo. The residue was taken up with chloroform. The organic layer was washed with saturated aqueous sodium carbonate, dried over magnesium sulfate, filtered off and concentrated in vacuo to give a crude product. The crude product was purified by column chromatography on silica gel with chloroform to give (3RS)-3-acetoxy-5-cyclohexyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05763437 |
|---|
| Source dataset | uspto-grants-1998_06 |
|---|
| ORD ID | ord-3709955e13d2435090da73d74c60e87d |
|---|
| Source note | uspto-grants-1998_06 |
|---|