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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39674생성일: 2026년 10월 23일

2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde → Tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/39674

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 248127—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물tert-Butyl 4-amino-4-methylpiperidine-1-carboxylateHCID 11310432—
용매Acetic AcidHCID 176—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidine-1-carboxylateHCID 59398035—

반응 단계

To 5 mL of a dichloromethane solution containing 0.50 g of tert-butyl 4-amino-4-methylpiperidine-1-carboxylate, 0.38 g of 2,3-dihydro-1,4-benzodioxin-6-carbaldehyde and 0.13 mL of acetic acid were added, and the mixture was stirred at room temperature for 3 hours. The reaction mixture was added with 0.74 g of sodium triacetoxyborohydride and stirred at the same temperature for 30 minutes. The reaction mixture was added with 0.74 g of sodium triacetoxyborohydride and stirred at the same temperature for 30 minutes, and then the reaction mixture was stirred for 1 hour under reflux by heating. Thereto were added chloroform and an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, and the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.81 g of a light brown oily substance, tert-butyl 4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)-4-methylpiperidine-1-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524738B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c846f63164644d04a5a0217a7ae5a053
출처 메모uspto-grants-2013_09