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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362366생성일: 2026년 10월 26일

Methylamine → (3-Chloro-benzofuran-2-ylmethyl)methylamine

https://huagongshe.com/reaction/1362366

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물Sodium borohydrideHCID 4311764—
반응물3-Chlorobenzofuran-2-carboxaldehydeHCID 4737020—
용매MethanolHCID 887—
생성물(3-Chloro-benzofuran-2-ylmethyl)methylamineHCID 5927758782.1%

반응 단계

To a solution of 3-chlorobenzofuran-2-carboxaldehyde (1.62 g, 8.9 mmol) in methanol (50 mL) is added N-methylamine (33% solution in ethanol, 1.11 g, 35.9 mmol) and stirred overnight at room temperature. The mixture is concentrated in vacuo, re-solvated in methanol (50 mL) and cooled in an ice bath. Sodium borohydride (407 mg, 10.8 mmol) is added in portions and the mixture stirred at room temperature for 4 h. The mixture is concentrated in vacuo, re-solvated in 1.3M sodium hydroxide solution, stirred for 20 min, extracted with ethyl acetate, dried with sodium sulfate and concentrated. Purification by column chromatography (silica, CH2Cl2/MeOH, 9/1) gave title compound (1.43 g, 82%) as a colorless oil. 1H NMR (300 MHz, DMSO-d6) δ 7.55-7.63 (m, 2H), 7.33-7.42 (m, 2H), 3.93 (s, 2H), 2.27 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-460640b88e1d4bb8977386d0a7e38603
출처 메모uspto-grants-2011_02