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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Methyl 3-hydroxy-4-iodobenzoate | HCID 10378812 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-hydroxy-4-[2-(trimethylsilyl)ethynyl]benzoate | HCID 22481756 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06828330B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-c6a9b2be08e849c1a9885f6719c14938 |
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| Source note | uspto-grants-2004_12 |
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