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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766916Generated: November 1, 2026

tert-Butyl hydroperoxide → Diallyl 2-[(tert-butyldimethylsilyl)oxymethyl]-6-methylbenzyl phosphate

https://huagongshe.com/reaction/1766916

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantDiallyl diisopropylphosphoramiditeHCID 4686855—
Reactant2-[(Tert-butyldimethylsilyl)oxymethyl]-6-methylbenzylalcoholHCID 21110453—
ReactantHCID 178418441HCID 178418441—
ProductDiallyl 2-[(tert-butyldimethylsilyl)oxymethyl]-6-methylbenzyl phosphateHCID 2111049488.4%

Reaction Steps

According to a similar procedure to that described in Example 1-(10), 2-[(tert-butyldimethylsilyl)oxymethyl]-6-methylbenzylalcohol (4.92 g, 18.5 mmol) obtained from Example 22-(2), tetrazole (3.23 g, 46.2 mmol), bis(allyloxy)(diisopropylamino)phosphine (described in Tetrahedron Lett., 30, 4219 (1989); 5.43 g, 22.2 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 (200 g) column (eluent; ethyl acetate:hexane=1:4˜2:3) to afford the title compound (6.03 g, 74% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230023B2
Source datasetuspto-grants-2007_06
ORD IDord-76e9d0215e2741908b8bc7d15b169001
Source noteuspto-grants-2007_06