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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium CarbonateHCID 11125—
ReactantLithium BromideHCID 82050—
Reactant3-nitro-6-bromo-6,7,8,9-tetrahydro [5H] benzocycloheptene-5-oneHCID 54277284—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product8,9-dihydro-3-nitro-5H-benzocyclohepten-5-oneHCID 2009473273.2%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04117164
Source datasetuspto-grants-1978_09
ORD IDord-e25981b1dd0e419b84b93f85781b0263
Source noteuspto-grants-1978_09