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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058Generated: October 23, 2026

(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propen-1-ol → (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrolein

https://huagongshe.com/en/reaction/1058

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propen-1-olHCID 19694368—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acroleinHCID 1969437889%

Reaction Steps

A mixture of (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propen-1-ol (3.85 g), activated manganese dioxide (8.00 g) and dichloromethane (150 ml ) was stirred at room temperature for 2 hours. After the insoluble portion was filtered off, the filtrate was concentrated to yield crystals of (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrolein (3.40 g, 89%), which was then recrystallized from dichloromethane-isopropyl ether to yield colorless prisms having a melting point of 132° to 133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723479
Source datasetuspto-grants-1998_03
ORD IDord-20c9273eacd748b48025e08d9d4eba7a
Source noteuspto-grants-1998_03