HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764720Generated: October 26, 2026
Water → 8,9-dihydro-3-nitro-5H-benzocyclohepten-5-one
https://huagongshe.com/reaction/1764720
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Carbonate | HCID 11125 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | 3-nitro-6-bromo-6,7,8,9-tetrahydro [5H] benzocycloheptene-5-one | HCID 54277284 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8,9-dihydro-3-nitro-5H-benzocyclohepten-5-one | HCID 20094732 | 73.2% |
Reaction Steps
A mixture of 548 g of lithium carbonate and 548 of lithium bromide in 5.480 liters of dimethylformamide was heated to 100° C. and 548 g of 3-nitro-6-bromo-6,7,8,9-tetrahydro [5H] benzocycloheptene-5-one were added thereto over 5 minutes. The mixture was held at 100° C. for 45 minutes and was then poured into 25 liters of a mixture of water and ice. The mixture was vacuum filterd and the insolubles were extracted 8 times with 1 liter of methylene chloride. The organic phase was washed with water, dried over sodium sulfate and was evaporated to dryness under reduced pressure to obtain a red crystalline mass. The latter was empasted successively 3 times with 400 ml of ether, once with 400 ml of ethanol and once with 400 ml of ether and was dried at 40° C. to obtain 286.7 g of 3-nitro-8,9-dihydro [5H] benzocycloheptene-5-one in the form of orange-red crystals melting at 128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04117164 |
|---|
| Source dataset | uspto-grants-1978_09 |
|---|
| ORD ID | ord-e25981b1dd0e419b84b93f85781b0263 |
|---|
| Source note | uspto-grants-1978_09 |
|---|