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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164830Generated: November 1, 2026

Potassium Hydroxide → 4-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene

https://huagongshe.com/reaction/2164830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant8-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene-5-oneHCID 20403345—
SolventEthylene GlycolHCID 174—
Product4-chloro-6,7-dihydro-5H-dibenzo[a,c]cyclohepteneHCID 13281339—

Reaction Steps

Under a dry nitrogen atmosphere a stirred mixture of 8-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene-5-one (2.6 grams, 0.011 mole), 85% hydrazine hydrate (5 ml, 0.1 mole), potassium hydroxide (4 grams, 0.071 mole) and ethylene glycol (30 ml) was heated at reflux for 1.5 hours. Sufficient volatiles were removed by distillation to increase the pot temperature to 200° while maintaining reflux. The two-phase reaction mixture was refluxed at that temperature for three hours. The mixture was cooled, poured into ice water, and the resultant mixture extracted with diethyl ether. The extract was washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated under reduced pressure to give a yellow oil. The oil was purified by distillation to give 4-chloro-6,7-dihydro-5H-dibenzo[a,c]cycloheptene (bp 119°-126°/0.15 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507317
Source datasetuspto-grants-1985_03
ORD IDord-c58b508672664ae9b5ad1d7c6a6f386c
Source noteuspto-grants-1985_03