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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977589Generated: October 29, 2026

HCID 15661774, compound → HCID 15661776, compound

https://huagongshe.com/reaction/977589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15661774HCID 15661774—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
ProductHCID 15661776HCID 1566177687.2%

Reaction Conditions

Temperature24 °C

Reaction Steps

11 g of manganese dioxide is added to a solution of 1.5 g of the above-produced benzyl alcohol in 30 ml of methylene chloride and stirred for 3 hours at 24° C. Then, it is filtered, washed with methylene chloride and concentrated by evaporation in a vacuum. 1.3 g of 3-[(1E,3E)-5-acetoxy-1,3-tridecadienyl]-benzaldehyde is obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614634
Source datasetuspto-grants-1997_03
ORD IDord-0ac518fc97c544dca38081cad9fc25fc
Source noteuspto-grants-1997_03