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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377080Generated: October 30, 2026

Dichloromethane → HCID 57009109, compound

https://huagongshe.com/reaction/377080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzoic acid, 2-chloro-, ion(1-)HCID 4368810—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 57213576HCID 57213576—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 57009109HCID 5700910970%

Reaction Steps

1.2 mg of DMAP and 0.9 ml of chlorophenylformate were added to a dichloromethane solution containing 1.12 g of a known (4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-1-hydroxy-7-methylcyclopenta[c]pyrane-4-carboxylic acid methylester followed by stirring for 1 hour at room temperature. The reaction mixture was then extracted with dichloromethane. After washing the organic phase with dilute hydrochloric acid and brine, it was dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel chromatography to obtain a colorless powder from the hexane-ethyl acetate eluate in the form of (1S,4aS,6S,7R,7aR)-6,7-epoxy-1,4a,5,6,7,7a-hexahydro-7-methyl-1-(phenoxycarbonyloxy)cyclopenta[c]pyrane-4-carboxylic acid methylester (1.16 g, yield: 70%). The physicochemical properties of this compound are as shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022888
Source datasetuspto-grants-2000_02
ORD IDord-2b05438048de4e7aa10bf7307e419070
Source noteuspto-grants-2000_02