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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929459Generated: October 25, 2026

Boron trifluoride → (S)-1-(tert-butyldimethylsilyloxy)-5-(trimethylsilyl)pent-4-yn-2-ol

https://huagongshe.com/reaction/929459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant(S)-Glycidoxy-t-butyldimethylsilaneHCID 10954307—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product(S)-1-(tert-butyldimethylsilyloxy)-5-(trimethylsilyl)pent-4-yn-2-olHCID 86667886—

Reaction Conditions

Temperature-78 °C

Reaction Steps

tert-Butyl lithium (2 eq) is added to a solution of TMS-acetylene (2 eq) in THF at −78° C. and the reaction mixture stirred for an additional 30 min. (S)-tert-butyldimethyl(oxiran-2-ylmethoxy)silane (1 eq) and BF3.EtO2 (2 eq) are added and stirred at −78° C. for 4.5 hours. The reaction is quenched by addition of aqueous ammonium chloride solution and extracted with ethyl acetate (3×). The combined organic layers are washed with brine, dried (MgSO4) and concentrated under reduced pressure to afford (S)-1-(tert-butyldimethylsilyloxy)-5-(trimethylsilyl)pent-4-yn-2-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296686B2
Source datasetuspto-grants-2016_03
ORD IDord-42a3b186073d4db1b47a7d9f79d75d78
Source noteuspto-grants-2016_03