HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537819Generated: October 26, 2026
Magnesium bromide diethyl etherate → Phytanyl Bromide
https://huagongshe.com/reaction/537819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Magnesium bromide diethyl etherate | HCID 9903262 | — |
| Reactant | Phytanyl Mesylate | HCID 60047967 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Phytanyl Bromide | HCID 10808570 | 90% |
Reaction Steps
To a suspension of magnesium bromide diethyl etherate (25.9 g, 100.3 mmol) in anhydrous diethyl ether (250 mL) under nitrogen at room temperature was added a solution of phytanyl mesylate (18.9 g, 50.2 mmol) in anhydrous diethyl ether (200 mL) dropwise over 15 minutes. The resulting slurry was stirred for 72 hours at room temperature. Upon completion, the reaction mixture was cooled to 0° C. and ice cold water was added dropwise until all solid dissolved and bubbling stopped. Diethyl ether (300 mL) was added, and the organic and aqueous layers separated. The aqueous layer was back-extracted with diethyl ether (200 mL). The combined diethyl ether extracts were dried on MgSO4, filtered, and concentrated. The resulting oil was purified by column chromatography (column 10″L×2″W; eluted with 100% hexanes) to afford the product as a pale yellow oil (16.3 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865675B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c79d6af0c51b458096e518832148653f |
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| Source note | uspto-grants-2014_10 |
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