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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128797Generated: October 30, 2026

Methyl 4-Formylbenzoate → methyl (E)-4-(4-phenyl-1-butenyl)benzoate

https://huagongshe.com/reaction/128797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-FormylbenzoateHCID 15294—
Reactant3-Phenylpropyl triphenylphosphonium bromideHCID 10928647—
Productmethyl (E)-4-(4-phenyl-1-butenyl)benzoateHCID 14183688—

Reaction Steps

Using the conditions in example 1(A), (3-phenylpropyl)triphenylphosphonium bromide and methyl 4-formylbenzoate are condensed, providing methyl (E)-4-(4-phenyl-1-butenyl)benzoate as a colorless oil after chromatographic separation from the later-eluting (Z) isomer. This is reduced with lithium aluminum hydride in THF in the usual fashion to provide (E)-4-(4-phenyl-1-butenyl)phenylmethanol as a colorless oil. Oxidation with pyridinium dichromate in the usual fashion provides (E)-4-(4-phenyl-1-butenyl)benzaldehyde as a colorless oil after chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464865
Source datasetuspto-grants-1995_11
ORD IDord-9187d2c11d8d4124a796dff270263da5
Source noteuspto-grants-1995_11