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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654761Generated: November 2, 2026

Benzaldehyde → 1-Phenyl-3-(trimethylsilyl)-2-propyn-1-ol

https://huagongshe.com/reaction/1654761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantDiethyl EtherHCID 3283—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyl-3-(trimethylsilyl)-2-propyn-1-olHCID 2760416100.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Place lithium hexamethyldisilazane (20 mL of a 1M solution in tetrahydrofuran, 20 mmol) under an argon atmosphere and cool to 0° C. Add, by dropwise addition, trimethylsilylacetylene (2.83 mL, 20 mmol) and stir for 1 hour at 0° C. Add benzaldehyde (2.03 mL, 20 mmol) in tetrahydrofuran (10 mL). Allow to warm to room temperature and stir for 1 hour. Pour the mixture into ethyl ether and water, separate the organic phase and evaporate the solvent in vacuo. Filter the oil through silica gel (20% ethyl acetate/hexane) and evaporate the solvent in vacuo to yield 4.09 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409942
Source datasetuspto-grants-1995_04
ORD IDord-499b7b88eb184209b78aee6d29f2b4f9
Source noteuspto-grants-1995_04