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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766921Generated: October 29, 2026

tert-Butyl hydroperoxide → HCID 46834505, compound

https://huagongshe.com/reaction/1766921

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantDiallyl diisopropylphosphoramiditeHCID 4686855—
ReactantHCID 15253504HCID 15253504—
ReactantHCID 178418441HCID 178418441—
ProductHCID 46834505HCID 4683450581%

Reaction Steps

According to a similar procedure to that described in Example 1-(10), [8-[(tert-butyldimethylsilyl)oxymethyl]-1-naphthyl]methanol (described in Aust. J. Chem., 49, 793 (1996); 4.04 g, 13.4 mmol), tetrazole (2.34 g, 33.4 mmol), bis(allyloxy)(diisopropylamino)phosphine (described in Tetrahedron Lett., 30, 4219 (1989); 3.93 g, 16.0 mmol), and tert-butyl hydroperoxide (80% di-tert-butyl peroxide solution; Merck; 1.8 g, 16 mmol) were reacted, and the reaction mixture was worked up to afford, after extraction, an oily residue. The residue was subjected to chromatography on a silica gel (120 g) column (eluent; ethyl acetate:hexane=1:5˜1:2) to afford the title compound (5.02 g, 81% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230023B2
Source datasetuspto-grants-2007_06
ORD IDord-7feebc360bea4bbdab8f1a82ed0301aa
Source noteuspto-grants-2007_06