HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638328Generated: October 31, 2026
Phenethyl bromide → HCID 13274713, compound
https://huagongshe.com/reaction/638328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Ethyl phosphorochloridite | HCID 68530 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13274713 | HCID 13274713 | — |
Reaction Steps
A suspension of 4.13 g (0.172 mol) of magnesium in 45 ml of dry ether under argon was treated with a solution of 31.2 g (0.168 mol) of 1-bromo-2-phenylethane (Aldrich) in 90 ml of dry ether, added at a rate that maintained reflux. The reaction was stirred overnight at room temperature under argon, then filtered under argon, cooled to 10° C. and treated with 26.3 g (0.168 mol) of diethyl chlorophosphonite (Aldrich) dissolved in 60 ml of dry ether, added slowly to keep the temperature near 10° C. After addition, the reaction was refluxed for 1 hour, filtered under argon and distilled at 1 atm to remove ether. Vacuum distillation of the residue gave 20.6 g (54%) of the title A compound which distilled at 94°-96° C./0.55 mm Hg. The 1H-NMR and 13C-NMR of this material were both consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560680 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-14eeea606cfa4876865a17cf0def3f5b |
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| Source note | uspto-grants-1985_12 |
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