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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249571Generated: October 29, 2026

Triethylamine → tert-Butyldimethyl-[1-(1-propylcyclobutyl)but-3-ynyloxy]silane

https://huagongshe.com/reaction/2249571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(1-Propylcyclobutyl)but-3-yn-1-olHCID 14254776—
SolventDichloromethaneHCID 6344—
Producttert-Butyldimethyl-[1-(1-propylcyclobutyl)but-3-ynyloxy]silaneHCID 15475299153.8%

Reaction Steps

t-Butyldimethylsilyltrifluoromethanesulfonate (1.8 mL, 7.88 mmol) was added to a solution of triethylamine (2.2 mL, 15.8 mmol) and alcohol 4 (650 mg, 3.94 mmol) in CH2Cl2 (5.0 mL) at 0° C. The reaction was stirred for 1 h and then saturated aqueous NaHCO3 was added. The mixture was extracted with CH2Cl2. The organic portion was washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. FCC (silica gel, 100% hexane) gave 1.7 g (100%) of the silyl ether 5 as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314890B2
Source datasetuspto-grants-2008_01
ORD IDord-0331834af2524f36beffdf98d9322b2e
Source noteuspto-grants-2008_01