Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793580Generated: November 2, 2026

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

https://huagongshe.com/reaction/1793580

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 numberUS07081463B2
Source datasetuspto-grants-2006_07
ORD IDord-72af2a30687844fa9df2bfb9b8bbf530
Source noteuspto-grants-2006_07