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HRID 277678作成日:2026年10月26日

4-Methylmorpholine → tert-butyl N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamate

https://huagongshe.com/reaction/277678

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium borohydrideHCID 4311764—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]carbamateHCID 2733675—

反応条件

温度0 °C

反応手順

To 5.7 g (0.023 mol) of Boc-PheOH dissolved in THF (30 mL) at −10° C. under N2 are added NMM (2.5 mL, 0.023 mol) and IBCF (3 mL, 0.023 mol). The reaction mixture is stirred for 15 minutes and filtered. The filtrate is slowly added to an ice-cold solution of NaBH4 (2.3 g, 0.061 mol) in H2O (10 mL) and then stirred for 1 hour at ice-bath temperature followed by stirring for 1 hour at room temperature. The reaction is cooled to 0° C., treated with saturated NaHCO3 solution, extracted with EtOAc, washed with 1M HCl, washed with water, dried over anhydrous MgSO4, and evaporated to dryness. The crude product is purified over a silica gel column eluted with 95:5 EtOAc/MeOH.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358928B1
出典データセットuspto-grants-2002_03
ORD IDord-ff64f4d6182e4e08be27bf3520af547f
出典メモuspto-grants-2002_03