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HRID 11207作成日:2026年10月24日

Bupropion Hydrochloride → alpha-Bromo-3-chloropropiophenone

https://huagongshe.com/ja/reaction/11207

反応式

関与物質

役割名称HCID仕込み量
反応物Bupropion HydrochlorideHCID 62884—
反応物Morpholin-4-olHCID 165345—
反応物3'-ChloropropiophenoneHCID 587128—
反応物1,4-Dioxane dibromideHCID 22225919—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物alpha-Bromo-3-chloropropiophenoneHCID 499211685%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098206B2
出典データセットuspto-grants-2006_08
ORD IDord-27b58087e3844fdf8b955fa933d6ceab
出典メモuspto-grants-2006_08