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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60250생성일: 2026년 10월 26일

Formaldehyde → (R)-tert-butyl 3-(hydroxymethyl)-4-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/60250

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sodium CarbonateHCID 10340—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물tert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820286—
용매MethanolHCID 887—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물(R)-tert-butyl 3-(hydroxymethyl)-4-methylpiperazine-1-carboxylateHCID 58365052—

반응 단계

To a solution of (R)-tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (115 mg, 0.53 mmol) in acetonitrile (1.4 mL) and water (0.3 mL) was added Formalin (0.11 mL, 1.6 mmol) followed by sodium triacetoxyborohydride (225 mg, 1.1 mmol). The reaction mixture was stirred for 20 minutes at ambient temperature. The reaction mixture was then basified via the addition of saturated aqueous sodium carbonate solution (1 mL), diluted with methylene chloride (50 mL) and methanol (5 mL), and washed with saturated aqueous sodium bicarbonate solution (2×15 mL). The organic layer was separated, dried over sodium sulfate, and concentrated in vacuo to afford a white crystalline solid, which was used in the next step without any further purification (120 mg, 98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440976B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-209d4574534a4c8dbaebce40c777f396
출처 메모uspto-grants-2016_09