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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243289Generated: November 1, 2026

Borane → Methyl 4-(4-bromo-2-formylbutyl)benzoate

https://huagongshe.com/reaction/2243289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
Reactant4-Bromo-2-[4-(methoxycarbonyl)benzyl]butanoic acidHCID 59210814—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(4-bromo-2-formylbutyl)benzoateHCID 17958613—

Reaction Steps

At 0° C., 10.7 g (33.95 mmol) of 4-bromo-2-[4-(methoxycarbonyl)benzyl]butanoic acid from Ex. VII in 200 ml of THF are treated with 40.74 ml (40.74 mmol) of a 1M solution of borane in THF, and the mixture is stirred with warming to room temperature for 2 hours. Excess borane is destroyed by addition of water. The mixture is extracted with ether and the organic phase is then dried over magnesium sulfate and the solvent is distilled off under reduced pressure. 10.23 g (33.92 mmol) of the highly unstable methyl 4-[4-bromo-2-(hydroxymethyl)butyl]benzoate remain, and this residue is immediately dissolved in 100 ml of methylene chloride and added dropwise to a suspension of 10.98 g (50.92 mmol) of pyridinium chlorochromate in 200 ml of methylene chloride. After 3.5 hours, the solution is filtered through silica gel which is washed thoroughly with ether, and the solvent is distilled off. The crude product is purified by flash chromatography on silica gel (0.04-0.063 nm) using methylene chloride/methanol 3/1 as mobile phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674825B2
Source datasetuspto-grants-2010_03
ORD IDord-2d364452a3aa4524bf33bd77b5a6125f
Source noteuspto-grants-2010_03