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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1366640생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1366640

반응식

참여 물질

역할이름HCID투입량
반응물(Phenylmethoxy)acetaldehydeHCID 108989—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물Benzyl (2S)-2-methylpiperazine-1-carboxylateHCID 40425199—
용매DichloromethaneHCID 6344—
생성물phenylmethyl (2S)-2-methyl-4-{2-[(phenylmethyl)oxy]ethyl}-1-piperazinecarboxylateHCID 6693599958%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07893056B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-ba015d2a15f246e69cfccaecc06d6998
출처 메모uspto-grants-2011_02