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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27964Generated: October 25, 2026

Hydrochloric Acid → gamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acid

https://huagongshe.com/reaction/27964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant(2-Carboxyethyl)triphenylphosphonium chlorideHCID 10270534—
Reactant9,10-Dihydro-9,10-methanoanthracene-9-carboxaldehydeHCID 12404141—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Productgamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acidHCID 54474651—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 9-formyl-9,10-dihydro-9,10-methanoanthracene (110 mg) and β-carboxyethyltriphenylphosphonium chloride (186 mg) in dimethylsulfoxide (2 ml) and tetrahydrofuran (2 ml) was added 65.4% sodium hydride dispersion in mineral oil (37 mg) at 0° C. under nitrogen. The reaction mixture was stirred at 0° C. for 6 hours, diluted with water, acidified with hydrochloric acid and extracted with benzene. The benzene extract was shaken with 2 N aqueous sodium hydroxide. The basic layer was acidified with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over anhydrous sodium sulfate and evaporated to dryness to give γ-(9,10-dihydro-9,10-methano-9-anthryl)-β-butenoic acid. M.P. 166°-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04224344
Source datasetuspto-grants-1980_09
ORD IDord-6a1bcab99e7646dca3cfbb7012c89a4b
Source noteuspto-grants-1980_09