HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405644Generated: October 23, 2026
Methyl 4-trimethylsilylethynylbenzoate → 4-(Trimethylsilylethynyl)benzyl alcohol
https://huagongshe.com/en/reaction/2405644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 4-trimethylsilylethynylbenzoate | HCID 640161 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Trimethylsilylethynyl)benzyl alcohol | HCID 11241165 | 93% |
Reaction Steps
Under argon condition, 4-((trimethylsilyl)ethynyl)benzoic acid methyl ester (316 mg, 1.36 mmol) was dissolved in 5 mL of dry THF and then cooled to 0° C. and LiAlH4 (2.04 mL, 1.0 M solution in THF, 2.04 mmol) was slowly added thereto. Upon completion of the reaction after stirring for 30 minutes at 0° C., the reaction was terminated by adding 77 μL of water, 154 μL of 10% aqueous sodium hydroxide solution and 231 μL of water in order. When the white viscous precipitate was produced, the mixture was filtered through silica pad to remove the precipitate. The resulting solution was concentrated by distillation under reduced pressure, and purified by column chromatography to obtain 258 mg (1.26 mmol, 93%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809012B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-d5ba5238ed624b6684e82be77b24e065 |
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| Source note | uspto-grants-2014_08 |
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