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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430744Generated: October 30, 2026

Hydrochloric Acid → HCID 67777371, compound

https://huagongshe.com/reaction/1430744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,10-PhenanthrolineHCID 1318—
Reactant10-Oxa-tricyclo[5.2.1.0*2,6*]dec-8-ene-3,5-dioneHCID 20679320—
ReactantHCID 178476525HCID 178476525—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 67777371HCID 67777371—

Reaction Steps

To a mixture of (1RS,2SR,6RS,7SR)-10-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione (374 mg, 2.3 mmol) and phenanthroline (610 mg, 5 mmol) under an atmosphere of nitrogen is added dry toluene (20 ml) and 4′-chloro-4-methylbiphen-3-yllead triacetate (2.0 g, 3.4 mmol). The reaction mixture is heated at reflux for 3.5 hours, then cooled to room temperature, acidified to pH1 with 2N aqueous hydrochloric acid (20 ml), ethyl acetate (20 ml) added 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-methylbiphenyl-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-4cf0a6eea0cf423781420c1640f7e618
Source noteuspto-grants-2015_01