HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl hydroperoxide → HCID 46834505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Diallyl diisopropylphosphoramidite | HCID 4686855 | — |
| Reactant | HCID 15253504 | HCID 15253504 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Product | HCID 46834505 | HCID 46834505 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230023B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-7feebc360bea4bbdab8f1a82ed0301aa |
| Source note | uspto-grants-2007_06 |