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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377072Generated: October 25, 2026

HCID 57263744, compound → (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy) cyclopenta [c]-pyrane-4-carboxylic acid

https://huagongshe.com/reaction/377072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57263744HCID 57263744—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
Product(1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy) cyclopenta [c]-pyrane-4-carboxylic acidHCID 18397301113.6%

Reaction Steps

35 mg of 5% palladium-carbon catalyst were added to an ethyl acetate solution containing 350 mg of (1S,4aS,6S,7R,7aR)-6,7-epoxy-7-methyl-1-(methylcarbamoyloxy)-1,4a,5,6,7,7a-hexahydrocyclopenta [c]-pyrane-4-carboxylic acid benzyl ester followed by stirring for 2 hours at room temperature under hydrogen gas atmosphere at 1 atm. After filtering out the insoluble matter, the filtrate was concentrated under reduced pressure to obtain a colorless powder in the form of (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(methylcarbamoyloxy) cyclopenta [c]-pyrane-4-carboxylic acid (298 mg; yield: 99%). The physicochemical properties of this compound are described in Table 1, Compound No. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022888
Source datasetuspto-grants-2000_02
ORD IDord-33fc9eeb98244a179812c4bf88624d62
Source noteuspto-grants-2000_02