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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869999Generated: October 30, 2026

Ethyl Acetate → {4-[5-Tert-butyl-4-isopropoxy-2-methyl-3-(3-trimethylsilanyl-prop-2-ynyl)-phenylethynyl]-phenyl}-acetic acid methyl ester

https://huagongshe.com/reaction/1869999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 57424261HCID 57424261—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
SolventTriethylamineHCID 8471—
Product{4-[5-Tert-butyl-4-isopropoxy-2-methyl-3-(3-trimethylsilanyl-prop-2-ynyl)-phenylethynyl]-phenyl}-acetic acid methyl esterHCID 8660019531.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

A solution of [4-(3-bromomethyl-5-tert-butyl-4-isopropoxy-2-methyl-phenylethynyl)-phenyl]-acetic acid methyl ester (Intermediate 148, 0.12 g, 0.25 mmol) in triethyl amine (1 mL) and N,N-dimethylformamide (4 mL) was sparged with argon and treated with trimethylsilylacetylene (0.5 mL, 3.5 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.025 g, 0.036 mmol). The resulting reaction mixture was heated at 85° C. overnight at the end of which it was cooled to ambient temperature and subjected to flash column chromatography over silica gel (230-400 mesh) using 4% ethyl acetate in hexane as the eluent followed by preparative normal phase HPLC using 3% ethyl acetate in hexane as the mobile phase to afford the title compound as an oil (0.038 g, 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638648B2
Source datasetuspto-grants-2009_12
ORD IDord-6abf8d9f90fa41f78b707863ed9bea73
Source noteuspto-grants-2009_12