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HRID 11208作成日:2026年10月23日

2-Amino-2-methyl-1-propanol → (2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol

https://huagongshe.com/ja/reaction/11208

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-2-methyl-1-propanolHCID 11807—
反応物alpha-Bromo-3-chloropropiophenoneHCID 4992116—
溶媒MethanolHCID 887—
生成物(2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinolHCID 994390875%

反応手順

To a solution of 2-bromo-3′-chloropropiophenone (19.3 g, 0.08 mol) in MeOH (100 mL) was added dropwise a solution of 2-amino-2-methyl-1-propanol (27.8 g, 0.31 mol) in methanol (200 mL) at ambient temperature. The mixture was stirred for 18 h and concentrated in vacuo. The residue was partitioned between water and diethyl ether. The combined organic phase was extracted with 10% aqueous hydrogen chloride. The combined aqueous acid extracts were chilled in an ice bath and made basic with 40% aqueous sodium hydroxide. The mixture was extracted with diethyl ether, the combined diethyl ether extracts were washed with water and saturated sodium chloride solution, dried (K2CO3) and concentrated in vacuo to give 15.0 g (75%) of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol as an off-white solid.

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-d55caad6b3ba44ea8fbfd252d937eada
出典メモuspto-grants-2006_08