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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 967377생성일: 2026년 10월 26일

Acetic Acid → tert-Butyl 4-(2-oxo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/967377

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물Methyl 2-aminobenzeneacetateHCID 5743389—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 4-(2-oxo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylateHCID 67472855130.2%

반응 단계

Methyl 2-aminophenylacetate (3.0 g, 18.2 mmol) and 1-tert-butoxycarbonyl-4-piperidone (4.5 g, 22.6 mmol) were set stirring in 50 mL of CH2Cl2 under an atmosphere of nitrogen. Sodium triacetoxyborohydride (5.4 g, 25.5 mmol) was added followed by 1 mL of acetic acid. After 20 h at rt the mixture was quenched by the slow addition of saturated NaHCO3. After stirring for 30 min, the organics were separated, dried (MgSO4), and evaporated to afford 7.5 g of a purple oil. Purification by column chromatography (silica, 10-50% EtOAc/hexanes) gave 3.9 g (62%) of the title compound. TLC (silica, 25% EtOAc/hexanes): Rf=0.15. 1H NMR (400 MHz, CDCl3): 7.25 (m, 2H), 7.01 (m, 2H), 4.40 (m, 1H), 3.53 (s, 2H), 2.83 (m, 2H), 2.32 (m, 2H), 1.70 (m, 2H), 1.51 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06953793B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-bfbb65c816a747f6b1f96984082eecfe
출처 메모uspto-grants-2005_10