Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841286Generated: November 3, 2026

Dimethylformamide → 5-Prop-2-en-1-ylidene-10,11-dihydro-5H-dibenzo(a,d)(7)annulene

https://huagongshe.com/reaction/1841286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)propyl methanesulfonateHCID 1712712—
ReactantEthyl 2-ethoxy-3-(4-hydroxyphenyl)propanoateHCID 11791243—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product5-Prop-2-en-1-ylidene-10,11-dihydro-5H-dibenzo(a,d)(7)annuleneHCID 61606070.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 5-(3-mesyloxypropylidene)-10,11-dihydro-dibenzo[a,d]cycloheptene (5.0 g, 15.2 mmol), ethyl 3-(4-hydroxyphenyl)-2-ethoxypropionate (3.7 g, 15.5 mmol), potassium carbonate (2.9 g, 21 mmol) and dimethylformamide (10 ml) was heated at 100° C. for 5 h. Benzene (200 ml) and water (200 ml) were added and the phases separated. The organic phase was dried, the solvent evaporated, and the product purified by chromatography on silica gel (benzene/chloroform eluent) to give first 2.5 g of 5-propenylidene-10,11-dihydro-5H-dibenzo(a,d)cycloheptene and then the title compound as an oil; 1.5 g (21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683111B2
Source datasetuspto-grants-2004_01
ORD IDord-98d20eddcae74c04a638268d77bf094a
Source noteuspto-grants-2004_01