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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913774Generated: November 2, 2026

Formic Acid → 4-[4-(tert-Butoxycarbonyl)phenyl]-2-[4-(methoxycarbonyl)benzyl]butanoic acid

https://huagongshe.com/reaction/1913774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantDiallyl {2-[4-(tert-butoxycarbonyl)phenyl]ethyl}[4-(methoxycarbonyl)benzyl]malonateHCID 59180509—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product4-[4-(tert-Butoxycarbonyl)phenyl]-2-[4-(methoxycarbonyl)benzyl]butanoic acidHCID 5918050070.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 0.79 ml (5.66 mmol) of triethylamine and 0.16 ml (4.29 mmol) of formic acid in 10 ml of dioxane is added to a solution of 920 mg (1.71 mmol) of diallyl {2-[4-(tert-butoxycarbonyl)phenyl]ethyl}[4-(methoxycarbonyl)benzyl]malonate, 31.5 mg (0.12 mmol) of triphenylphosphine and 7.7 mg (0.03 mmol) of palladium acetate in 10 ml of dioxane at room temperature. The reaction mixture is then stirred at 100° C. for 12 hours. After conversion is complete, the reaction solution is cooled and the solvent is removed in vacuo. The resulting residue is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 4:1→1:1). 497 mg (1.2 mmol, 61% yield) of a colourless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609727B2
Source datasetuspto-grants-2013_12
ORD IDord-a52f1a2c8080404ba05a72dfe7f94282
Source noteuspto-grants-2013_12