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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430751Generated: October 29, 2026

Hydrochloric Acid → HCID 75288490, compound

https://huagongshe.com/reaction/1430751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroformHCID 6212—
Reactant10-Oxa-tricyclo[5.2.1.0*2,6*]dec-8-ene-3,5-dioneHCID 20679320—
ReactantHCID 178476534HCID 178476534—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
ProductHCID 75288490HCID 75288490—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a mixture of (1RS,2SR,6RS,7SR)-10-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione (1.7 g, 0.01 mol), 4-dimethylaminopyridine (5.0 g, 0.04 mol) and 4′-chloro-4-ethylbiphen-3-yllead triacetate (9.2 g, 0.015 mol) under an atmosphere of nitrogen is added dry chloroform (50 ml)). The reaction mixture is heated at 40° C. for 5 hours, then cooled to room temperature. The mixture is diluted with ethyl acetate (50 ml), acidified with 2N aqueous hydrochloric acid (50 ml), and the mixture is filtered to remove solids. The filtrate is poured into a separating funnel and extracted with ethyl acetate. The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The crude product is purified by column chromatography on silica gel to give (1RS,2SR,6RS,7SR)-4-(4′-chloro-4-ethylbiphen-3-yl)-10-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940913B2
Source datasetuspto-grants-2015_01
ORD IDord-dacd2030ac6149f7b132a0e0216b196a
Source noteuspto-grants-2015_01