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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475736Generated: November 1, 2026

Sodium Bicarbonate → tert-Butyl-dimethyl-[2-(3-oxetan-3-yl-phenyl)-ethoxy]-silane

https://huagongshe.com/reaction/1475736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant3-IodooxetaneHCID 13356686—
Reactant3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-benzeneboronic AcidHCID 58845136—
CatalystNickel(II) iodideHCID 26038—
Catalyst(1R,2R)-2-AminocyclohexanolHCID 735777—
SolventIsopropanolHCID 3776—
Producttert-Butyl-dimethyl-[2-(3-oxetan-3-yl-phenyl)-ethoxy]-silaneHCID 67170174—

Reaction Steps

4.6 g of 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-phenylboronic acid, 130 mg of nickel iodide, 5.0 g of sodium bis(trimethylsilyl)amide and 62 mg of (1R,2R)-2-aminocyclohexanol were placed in a microwave vial and 3.5 ml of isopropanol were added. The mixture was stirred for 10 min at room temperature. Then a solution of 3-iodooxetane in 1.5 ml of isopropanol was added and the mixture treated under microwave irradiation at 80° C. for 30 min. The obtained mixture was combined with the mixtures obtained in three further runs of the synthesis, poured into 50 ml of a saturated aqueous sodium hydrogencarbonate solution and extracted three time with 50 ml each of EA. The combined organic layers were dried with magnesium sulfate and evaporated to yield 9.0 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018383B2
Source datasetuspto-grants-2015_04
ORD IDord-60e1331a1e364d2aab6a02e7ef27b15f
Source noteuspto-grants-2015_04