Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981184Generated: October 27, 2026

Ethanol → Diethyl 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-malonate

https://huagongshe.com/reaction/1981184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiethyl MalonateHCID 7761—
Reactant5H-Dibenzo(a,d)cycloheptene, 10,11-dihydro-5-chloro-HCID 14587—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-malonateHCID 20187928—

Reaction Steps

A mixture of 11.4 g of magnesium shavings, 151.5 g of diethyl malonate and 300 ml of dry ethanol is warmed to 60° under argon over a period of 30 minutes. After the vigorous reaction has faded, the mixture is heated to boiling under reflux for an additional 1 hour and then concentrated in vacuo. The residue is treated twice with 300 ml of dry benzene each time and in each case evaporated well. The residue obtained is dissolved under argon in 350 ml of dry tetrahydrofuran. Thereto there is added dropwise at room temperature over a period of 20 minutes a solution of 195.5 g of 5-chloro-10,11-dihydro-5H-dibenzo[a,d]cycloheptene in 500 ml of dry tetrahydrofuran. The mixture is heated to boiling under reflux overnight while stirring and then evaporated in vacuo. The residue obtained is partitioned between 2.0 l of toluene and 500 ml of ice-water. The organic phase is washed successively twice with 500 ml of 1N hydrochloric acid each time, twice with 500 ml of water each time, twice with 250 ml of saturated sodium bicarbonate solution each time and several times with water, dried over magnesium sulfate and evaporated in vacuo. Diethyl 10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-malonate is obtained as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04513002
Source datasetuspto-grants-1985_04
ORD IDord-dc51706c71f6475e89b400a137b85054
Source noteuspto-grants-1985_04