HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 17-Bromoheptadec-6-en-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 11-Bromo-1-undecanol | HCID 74163 | — |
| Reactant | Phosphonium, (6-hydroxyhexyl)triphenyl-, bromide | HCID 2784664 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 17-Bromoheptadec-6-en-1-ol | HCID 53688827 | 45.8% |
Reaction Steps
A solution of (6-hydroxyhexyl)triphenylphosphonium bromide (5.0 g) in dichloromethane (20 ml) was added dropwise to a mixture of potassium tertiary-butoxide (2.8 g) in tetrahydrofuran (100 ml) at 5°. After ten minutes, 11-bromoundecanol (2.8 g) in tetrahydrofuran (20 ml) was added and the reaction stirred at 5° until TLC indicated completion of the reaction. Water (20 ml) was added and the mixture then concentrated in vacuo. Water (20 ml) was added to the residue and the aqueous phase extracted with ether (2×50 ml). The combined organic extracts were dried (MgSO4) and concentrated in vacuo to give a brown oil. This was subjected to column chromatography to yield 17-bromoheptadec-6-en-1-ol (1.7 g, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441731 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-3d8c8c6c97a24d6d99f70e7075a22ca2 |
| Source note | uspto-grants-1995_08 |