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HRID 1026783作成日:2026年10月27日

Toluene → (2S,3R)-3-(3-Amino-phenyl)-1-(dimethylamino)-2-methyl-pentan-3-ol

https://huagongshe.com/reaction/1026783

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Ammonium bisulfateHCID 24655—
反応物(S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-oneHCID 53235125—
反応物HCID 178418443HCID 178418443—
溶媒TetrahydrofuranHCID 8028—
生成物(2S,3R)-3-(3-Amino-phenyl)-1-(dimethylamino)-2-methyl-pentan-3-olHCID 7066450461.2%

反応手順

726 ml of ethylmagnesium bromide (1M in THF; 0.726 mol) are added under a nitrogen flow into a 2-liter four-neck flask, provided with mechanical stirrer, thermometer and dropping funnel. A solution of (S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-one (50 g, 0.242 mol) in 50 ml of THF are dripped maintaining the temperature between 15-30° C. The reaction is stirred at room temperature for 3 hours. It is cooled to about 10° C. and toluene (200 ml) and slowly a 20% ammonium hydrogen sulphate solution (200 ml) are added. The mixture is stirred for 30 minutes and the phases are separated after about 15 minutes of rest. The organic phase is concentrated under vacuum almost to oily residue. Then toluene (200 ml), 30% sodium metabisulfite solution (300 ml) are added. The mixture is stirred for 30 minutes and the phases are separated after about 15 minutes of rest. The aqueous phase is washed 2 times with 200 ml of toluene. The organic phases are eliminated while Cert-butylmethylether (200 ml) is added to the aqueous phase. The pH of the mixture is brought to 11-12 with 28% sodium hydroxide. The mixture is stirred for 30 minutes and the phases are separated after about 15 minutes of rest. The aqueous phase is eliminated while the organic phase is concentrated under vacuum to oily residue which solidifies by cooling. 35 g of a yellowish solid with a 95% HPLC purity are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08729308B2
出典データセットuspto-grants-2014_05
ORD IDord-2be645676eda4e9e9986508764467296
出典メモuspto-grants-2014_05