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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934564Generated: November 1, 2026

HCID 86758055, compound → HCID 57168096, compound

https://huagongshe.com/reaction/1934564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86758055HCID 86758055—
ReactantHCID 86758056HCID 86758056—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 57168096HCID 57168096—
ProductHCID 86758055HCID 86758055—

Reaction Steps

To a solution of a mixture of ethyl {[6-(N,N-diphenyl-carbamoyloxy)methyl-5,6-epoxy-6,7,8,9-tetrahydro-5H-benzo-cyclohepten-5-yl]oxy}acetate and ethyl {[6-(N,N-diphenyl-carbamoyloxy) methyl-6,7-epoxy-6,7,8,9-tetrahydro-5H-benzo-cyclohepten-1-yl]oxy}acetate (265 mg) in EtOAc (13 ml) was added 10% Pd—C (wet) (80 mg). The mixture was stirred under hydrogen atmosphere at room temperature for 6 hours. After removal of the catalyst by filtration, the filtrate was evaporated. The residue was purified by silica gel column chromatography (hexane-EtOAc 2:1 to 1:1) to give ethyl {[6-(N,N-diphenylcarbamoyloxy)methyl-6-hydroxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yl]oxy}acetate (193.3 mg) as a solid and ethyl {[6-(N,N-diphenylcarbamoyloxy) methyl-6,7-epoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-1-yl]oxy}acetate (60.0 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384072B1
Source datasetuspto-grants-2002_05
ORD IDord-cb888c23f2ca49b5a2ef5c167ef7957d
Source noteuspto-grants-2002_05