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HRID 1366640作成日:2026年10月27日

(Phenylmethoxy)acetaldehyde → phenylmethyl (2S)-2-methyl-4-{2-[(phenylmethyl)oxy]ethyl}-1-piperazinecarboxylate

https://huagongshe.com/reaction/1366640

反応式

関与物質

役割名称HCID仕込み量
反応物(Phenylmethoxy)acetaldehydeHCID 108989—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Benzyl (2S)-2-methylpiperazine-1-carboxylateHCID 40425199—
溶媒DichloromethaneHCID 6344—
生成物phenylmethyl (2S)-2-methyl-4-{2-[(phenylmethyl)oxy]ethyl}-1-piperazinecarboxylateHCID 6693599958%

反応手順

A solution of phenylmethyl (2S)-2-methyl-1-piperazinecarboxylate (commercially available) (1 g, 4.3 mmol) and benzyloxyacetaldehyde (0.9 mL, 6.4 mmol) in DCM (50 mL) was stirred for 30 minutes, and then NaBH(OAc)3 (1.36 g, 6.4 mmol) was added. The reaction was stirred overnight before being quenched with 1 M NaOH. The phases were separated and the aqueous layer was extracted with DCM. The combined organics were washed with brine, dried over sodium sulfate and concentrated to a crude residue, which was purified by silica gel chromatography (5-95% EtOAc in hexane) yielding phenylmethyl (2S)-2-methyl-4-{2-[(phenylmethyl)oxy]ethyl}-1-piperazinecarboxylate (0.93 g, 58%). LCMS: (M+H)+: 369.1

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893056B2
出典データセットuspto-grants-2011_02
ORD IDord-ba015d2a15f246e69cfccaecc06d6998
出典メモuspto-grants-2011_02