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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113247Generated: October 30, 2026

1-methoxy-5-(2-propenyl)-2-oxabicyclo[3.3.0]octane → HCID 57644359, compound

https://huagongshe.com/reaction/2113247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-methoxy-5-(2-propenyl)-2-oxabicyclo[3.3.0]octaneHCID 11298330—
SolventMethanolHCID 887—
ProductHCID 57644359HCID 5764435996%

Reaction Steps

0.01 part of Lindler catalyst (manufactured by Aldrich Co.) was added to a solution of 0.2 part of a diastereomer (Isomer 5) of 1-methoxy-5-(2-propenyl)-2-oxabicyclo[3.3.0]octane obtained in Example 6 in 8 parts of methanol. The hydrogenation reaction was carried out at room temperature in a nitrogen atmosphere under a small hydrogen pressure for two hours. After the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to obtain 0.2 part of one diastreomer (Isomer 7) of the target 1-methoxy-5-n-propyl-2-oxabicyclo[3.3.0]octane as a colorless oil (yield: 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524978B2
Source datasetuspto-grants-2009_04
ORD IDord-591e34b58590467b870e0ae9a0b15dde
Source noteuspto-grants-2009_04