Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Magnesium Bromide | HCID 82241 | — |
| Reactant | Phytanyl Mesylate | HCID 60047967 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Phytanyl Bromide | HCID 10808570 | — |
Reaction Steps
Magnesium bromide etherate (17 g, 55 mmol) and a stir bar were added to a 500 mL round bottom flask. The flask was sealed and flushed with nitrogen and anhydrous diethyl ether (200 mL) added via cannula. A solution of phytanyl mesylate (10.9 g, 28.9 mmol (FW=377)) in anhydrous ether (50 mL) was also added via canulla, and the suspension stirred overnight. The following morning a precipitate had formed on the side of the flask. Chilled water (200 mL) was added (ppte dissolved) and the mixture transferred to a 1000-mL separating funnel. After shaking, the organic phase was separated. The aqueous phase was then extracted with ether (2×150 mL) and all ether phases combined. The ether phase was washed with water (2×150 mL), brine (150 mL) and dried over anhydrous Mg2SO4. The solution was filtered, concentrated, and purified by flash chromatography. Final yield 9.5 g (26.3 mmol, 91.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09187748B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-3d30adc9400147bebc6bc3886657d5d9 |
|---|
| Source note | uspto-grants-2015_11 |
|---|