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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-trimethylsilylethynylbenzoateHCID 640161—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4-(Trimethylsilylethynyl)benzyl alcoholHCID 1124116593%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809012B2
Source datasetuspto-grants-2014_08
ORD IDord-d5ba5238ed624b6684e82be77b24e065
Source noteuspto-grants-2014_08