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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623034Generated: November 1, 2026

Triacetoxyperiodinane → 8-(Tert-butyl-dimethyl-silanyloxymethyl)-naphthalene-1-carbaldehyde

https://huagongshe.com/reaction/1623034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant[8-(tert-Butyl-dimethyl-silanyloxymethyl)-naphthalen-1-yl]-methanolHCID 137328532—
SolventDichloromethaneHCID 6344—
Product8-(Tert-butyl-dimethyl-silanyloxymethyl)-naphthalene-1-carbaldehydeHCID 137328531—

Reaction Steps

[8-(tert-Butyl-dimethyl-silanyloxymethyl)-naphthalen-1-yl]-methanol (Aust. J. Chem. 1996, 49, 793-800) (0.2 g, 0.66 mmol) was dissolved in dichloromethane (8 mL). To the solution was then added 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one, also known as Dess-Martin periodinane (0.56 g, 1.32 mmol). The reaction mixture was stirred for 1 hr then partitioned with an aqueous saturated solution of thiosulfate and dichloromethane. The organic layer was washed with an aqueous saturated solution of thiosulfate, an aqueous saturated solution of sodium bicarbonate, brine, dried with Na2SO4, filtered and the solvent evaporated in vacuo to yield a crude oil. The crude oil was purified via flash chromatography (6.0% ammonia 2.0 M in methanol/dichloromethane) to yield 8-(tert-butyl-dimethyl-silanyloxymethyl)-naphthalene-1-carbaldehyde as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778956B2
Source datasetuspto-grants-2014_07
ORD IDord-14e14d851f71423f9c14b38fe77f1a36
Source noteuspto-grants-2014_07