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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308846Generated: November 2, 2026

Ethylene Oxide → 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-ethanol

https://huagongshe.com/reaction/2308846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
Reactant10,11-dihydro-5H-dibenzo(a,d)cyclohepteneHCID 70029—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-ethanolHCID 18521517—

Reaction Steps

A solution of 58.3 g of dibenzosuberane in 750 ml of tetrahydrofuran, stirred under argon, is cooled to about 10° in an ice-bath and treated dropwise with 190 ml of an about 2M solution of butyl lithium in hexane. The dark red solution is heated to boiling under reflux for 2 hours. Ethylene oxide is conducted for 15 minutes into the solution, cooled to about 10°, subsequently the mixture is stirred at room temperature for 1 hour and finally heated to boiling under reflux for an additional 30 minutes. The cooled mixture is poured into 300 ml of ice-cold 3N hydrochloric acid and extracted twice with 2 l of ether each time. The organic extracts are washed with 500 ml of 2N potassium bicarbonate solution, combined, dried over magnesium sulfate and evaporated. The residue is boiled up three times with 50 ml of pentane each time. There is obtained 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-ethanol in the form of a very viscous, yellowish oil, Rf: 0.25 (toluene/ethyl acetate, 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04691040
Source datasetuspto-grants-1987_09
ORD IDord-9b15e1ed18e14587a9685b1aaffce836
Source noteuspto-grants-1987_09