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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727230Generated: October 26, 2026

5H-Dibenzo[a,d]cyclohepten-5-one → 5-cyclopropyl-5H-dibenzo[a,d]cyclohepten-5-ol

https://huagongshe.com/reaction/727230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5H-Dibenzo[a,d]cyclohepten-5-oneHCID 16679—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418630HCID 178418630—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-cyclopropyl-5H-dibenzo[a,d]cyclohepten-5-olHCID 18799338—

Reaction Steps

A solution of cyclopropylmagnesium bromide in dry THF (prepared from cyclopropylbromide (8.0 g, 0.067 mol), magnesium turnings (1.3 g, 0.053 mol) and dry THF (35 ml)) was placed under an atmosphere of nitrogen. A solution of 5H-dibenzo[a,d]cyclohepten-5-one (6.0 g, 0.028 mol) in dry THF (15 ml) was added dropwise and when addition was complete the mixture was heated at reflux for 30 minutes. The reaction mixture was cooled on an ice-bath and saturated ammonium chloride (35 ml) was carefully added. The mixture was diluted with water (50 ml) and extracted with diethyl ether (2×50 ml). The combined organic extracts were washed with water, dried (Na2SO4) and the solvent was evaporated in vacuo to give 8.6 g of crude 5-cyclopropyl-5H-dibenzo[a,d]cyclohepten-5-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712292
Source datasetuspto-grants-1998_01
ORD IDord-9b3df842558846298b989e95b69c9c20
Source noteuspto-grants-1998_01