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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729776Generated: October 30, 2026

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

https://huagongshe.com/reaction/729776

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 numberUS07582649B2
Source datasetuspto-grants-2009_09
ORD IDord-f8d5453d49a64d47aff283c5fce0dc7d
Source noteuspto-grants-2009_09