HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl hydroperoxide → Diallyl 2-[(tert-butyldimethylsilyl)oxymethyl]-6-methylbenzyl phosphate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Diallyl diisopropylphosphoramidite | HCID 4686855 | — |
| Reactant | 2-[(Tert-butyldimethylsilyl)oxymethyl]-6-methylbenzylalcohol | HCID 21110453 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Product | Diallyl 2-[(tert-butyldimethylsilyl)oxymethyl]-6-methylbenzyl phosphate | HCID 21110494 | 88.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07230023B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-76e9d0215e2741908b8bc7d15b169001 |
| Source note | uspto-grants-2007_06 |