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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1843968생성일: 2026년 10월 27일

Acetic Acid → 3-Bromo-4-(pyrrolidin-1-ylmethyl)pyridine

https://huagongshe.com/reaction/1843968

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PyrrolidineHCID 31268—
반응물3-Bromopyridine-4-carboxaldehydeHCID 2762997—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물3-Bromo-4-(pyrrolidin-1-ylmethyl)pyridineHCID 5963613696.52%

반응 단계

Catalytic amount of acetic acid (0.3 mL) was added to a mixture of 3-bromoisonicotinaldehyde (200 mg, 1.075 mmol) and pyrrolidine (0.12 mL, 1.34 mmol) in DCE (20 mL) under nitrogen atmosphere and the resulting mixture was stirred at room temperature for 2.3 hours. This was followed by the addition of sodium triacetoxy-borohydride (342 mg, 1.612 mmol) at 0° C. The reaction mixture was stirred at room temperature overnight. The reaction was monitored by TLC (50% ethylacetate in hexane). The reaction mixture was washed with NaHCO3 solution and separated the layers. The organic layer was dried over Na2SO4 and concentrated to afford 250 mg of the product (96.52% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08946260B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-e993270ffbbd4f8f8c0f75807bf2bc26
출처 메모uspto-grants-2015_02