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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902622Generated: October 30, 2026

{3-[4-(t-Butyldimethylsilylhydroxy)but-1-ynyl]phenyl}acetic acid methyl ester → {3-[4-Hydroxybutyl]phenyl)acetic acid methyl ester

https://huagongshe.com/reaction/902622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{3-[4-(t-Butyldimethylsilylhydroxy)but-1-ynyl]phenyl}acetic acid methyl esterHCID 69253921—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product{3-[4-Hydroxybutyl]phenyl)acetic acid methyl esterHCID 5974506464.3%

Reaction Steps

A solution of {3-[4-(t-butyidimethylsilyloxy)but-1-ynyl]phenyl}acetic acid methyl ester (700 mg, 2.1 mmol) in MeOH (15 ml) was treated with 5% Pd/C (100 mg) and hydrogen gas (1 atm) for 1 hr. The catalyst was filtered, and the solvent evaporated. The residue was dissolved in THF (1 ml), and treated with tetrabutyl ammonium fluoride (2 ml of a 1N solution in THF) for 2 hr. The reaction was diluted with water and extracted with diethyl ether. The organic extracts were washed with water, dried, evaporated, and the volatile organics removed by vacuum to give the title compound as an oil (300 mg, 64%). MS (ESI) 223.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365085B2
Source datasetuspto-grants-2008_04
ORD IDord-3e90e4209aa043d4a3e92a1e8dc2b895
Source noteuspto-grants-2008_04