HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 86758464, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 23245531 | HCID 23245531 | — |
| Reactant | HCID 178418395 | HCID 178418395 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86758464 | HCID 86758464 | — |
Reaction Steps
To a solution of 6.59 g of 2-mercapto-benzothiazole and 7.87 g of triphenylphosphine in 65 ml of THF was added at 0° a solution of 9.25 g of (2E,9Z)-12,12,12-Trifluoro-7,7-dimethyl-11-triethylsilanyloxy-11-trifluoromethyl-dodeca-2,9-dien-1-ol in 35 ml of THF which was followed by addition of 8.09 g of diisopropyl azodicarboxylate over 20 min and stirring was continued at 0° for 1 h after which time t.l.c. indicated completion of the reaction. The mixture was washed with sat. aqueous NH4Cl- and NaCl-solution, the organic layer was dried over MgSO4 and evaporated. The residue was chromatographed on silica with hexane/AcOEt 9:1 to give 11.13 g of the pure (t.l.c.) title compound as a yellow oil. IR (neat): 1663w (C═C). MS (EI): 611/7 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06437142B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-4acc82e6ee954bca93ecf73f92a8498d |
| Source note | uspto-grants-2002_08 |