HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635480Generated: October 30, 2026
Phenethyl bromide → HCID 22618832, compound
https://huagongshe.com/reaction/635480
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1,5-Bis(benzyloxy)pentan-3-one | HCID 22618787 | — |
| Reactant | HCID 178419670 | HCID 178419670 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22618832 | HCID 22618832 | — |
Reaction Steps
To a solution of 1,5-dibenzyloxy-3-pentanone (13.9 g) in tetrahydrofuran (150 ml) was dropwise added a solution of 2-phenylethyl-magnesium bromide, which was prepared from 2-phenylethyl bromide (24 g) and magnesium (3.1 g), in tetrahydrofuran (100 ml) under ice-cooling. The mixture was stirred under ice-cooling for 90 minutes, poured into a saturated aqueous ammonium chloride solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium hydrogencarbonate solution and a saturated brine, dried over anhydrous sodium sulfate, and concentrated. The residue obtained was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=4:1) to give the subject compound (8.1 g) as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187821B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-b020010bbda0458ab007c5cab772613e |
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| Source note | uspto-grants-2001_02 |
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