HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650503Generated: October 25, 2026
Bupropion Hydrochloride → alpha-Bromo-3-chloropropiophenone
https://huagongshe.com/reaction/650503
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bupropion Hydrochloride | HCID 62884 | — |
| Reactant | Morpholin-4-ol | HCID 165345 | — |
| Reactant | 3'-Chloropropiophenone | HCID 587128 | — |
| Reactant | 1,4-Dioxane dibromide | HCID 22225919 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | alpha-Bromo-3-chloropropiophenone | HCID 4992116 | 85% |
Reaction Steps
The racemate of the morpholinol metabolite of bupropion hydrochloride ((+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride) may be synthesized by the following process. To 3′-chloropropiophenone (10.0 g, 0.06 mol) in dioxane (50 mL) was added a solution of dioxane dibromide (14.9 g, 0.06 mol) in dioxane (50 mL). The reaction mixture was stirred for 2h at ambient temperature and poured into a mixture of ice and water (500 mL). The mixture was extracted several times with methylene chloride. The combined extracts were dried (Na2SO4) and concentrated in vacuo to give 14.8 g (85%) of 2-bromo-3′-chloropropiophenone as a pale yellow oil. This was used without further purification. NMR (300 Mhz, CDCl3); δ 7.99 (m, 1H), 7.90 (d, 1H), 7.57 (d, 1H), 7.44 (t, 1H), 5.22 (q, 1H), 1.91 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06274579B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-b5cf799993054d45a59d96f5f194ab64 |
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| Source note | uspto-grants-2001_08 |
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