Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 58250163 | HCID 58250163 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58250153 | HCID 58250153 | 66% |
Reaction Steps
Tetrabutylammonium fluoride (1 M solution in THF, 0.764 mL, 0.764 mmol) was added drop wise to a stirred solution of tert-butyldiphenyl((17Z,20Z,23Z,26Z)-12-(phenylsulfonyl)dotriaconta-17,20,23,26-tetra-enyloxy)silane (0.16 g, 0.191 mmol) in dry THF (2 mL) and stirring was continued for 1 h. Upon completion of reaction as judged y TLC, water (3 mL) was added and the reaction mixture was extracted with ethyl acetate (3×15 mL). The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude was purified by silica gel column chromatography using 30% ethyl acetate/hexane to afford the title product as a clear oil (0.075 g, 66%). 1H NMR (CDCl3): δ7.88 (d, 2H, J=7.2 Hz), 7.57 (m, 3H), 5.38 (m, 8H), 3.65 (br s, 2H), 2.81 (m, 7H), 2.05 (m, 4H), 1.81 (m, 2H), 1.37-1.20 (m, 30H), 1.04 (t, 3H, J=6.9 Hz). m/z (APCI) 599.45 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08563760B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-e254c83a39324f919d2612c67e6258b0 |
|---|
| Source note | uspto-grants-2013_10 |
|---|