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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11207Generated: October 26, 2026

Bupropion Hydrochloride → alpha-Bromo-3-chloropropiophenone

https://huagongshe.com/reaction/11207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBupropion HydrochlorideHCID 62884—
ReactantMorpholin-4-olHCID 165345—
Reactant3'-ChloropropiophenoneHCID 587128—
Reactant1,4-Dioxane dibromideHCID 22225919—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Productalpha-Bromo-3-chloropropiophenoneHCID 499211685%

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 2 h 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098206B2
Source datasetuspto-grants-2006_08
ORD IDord-27b58087e3844fdf8b955fa933d6ceab
Source noteuspto-grants-2006_08