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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306658Generated: October 26, 2026

Trimethylsilylacetylene → Methyl 3-hydroxy-4-[2-(trimethylsilyl)ethynyl]benzoate

https://huagongshe.com/reaction/2306658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantMethyl 3-hydroxy-4-iodobenzoateHCID 10378812—
CatalystHCID 178418476HCID 178418476—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-hydroxy-4-[2-(trimethylsilyl)ethynyl]benzoateHCID 2248175691%

Reaction Conditions

Temperature50 °C

Reaction Steps

Methyl 3-hydroxy-4-iodobenzoate (5.22 g, 18.8 mmol) is combined with trimethylsilylacetylene (3.71 mL, 26.3 mmol), bis(triphenylphosphine)palladium dichloride (386 mg, 0.55 mmol) and cuprous iodide (54 mg, 0.28 mmol) in THF (20 mL) CHCl3 (40 mL) in a dry flask, under nitrogen. TEA (8.14 mL<58.4 mmol) is added and the mixture is heated to 50° C. for 4 h. The mixture is diluted with CHCl3 (60 mL), washed with 5% HCl (2×40 mL), dried over anhydrous MgSO4 and concentrated to a brown paste (8.31 g). The crude material is chromatographed over a standard 90 g Biotage column, eluting with 10% EtOAc/hexane (1 L) followed by 15% EtOAc/hexane (1 L). The appropriate fractions are combined and concentrated to afford 4.22 g (91%) of methyl 3-hydroxy-4-[(trimethylsilyl)ethynyl]benzoate as a yellow solid. HRMS (FAB) calcd for C13H16O3SI+H1: 249.0947, found 249.0947.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828330B2
Source datasetuspto-grants-2004_12
ORD IDord-c6a9b2be08e849c1a9885f6719c14938
Source noteuspto-grants-2004_12