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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2097156생성일: 2026년 10월 26일

Water → 1-(benzofuran-5-yl)-N-methylmethanamine

https://huagongshe.com/reaction/2097156

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물MethylamineHCID 6329—
반응물1-Benzofuran-5-carbaldehydeHCID 2773875—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물1-(benzofuran-5-yl)-N-methylmethanamineHCID 2184361991%

반응 단계

Benzofuran-5-carbaldehyde (315 mg, 2.16 mmol) was dissolved in anhydrous methanol (10 mL). Methylamine (0.86 mL of 33% solution in ethanol, 6.91 mmol) was added and the reaction was stirred for 3 h. The solution was concentrated to a brown oil and then dissolved in anhydrous methanol (10 mL). Sodium borohydride (83.2 mg, 2.20 mmol) was added and the mixture was stirred overnight at room temperature. Water (5 mL) was added and the solution was concentrated. Sodium hydroxide (10 mL, 1N) was added and the aqueous layer was extracted with ethyl acetate (3×20 mL). Combined organic layers were dried over MgSO4, filtered and concentrated to afford benzofuran-5-yl-N-methylmethanamine (316 mg, 91%) as a light brown oil: 1H NMR (400 MHz, DMSO-d6) δ 7.93 (s, 1H), 7.56 (s, 1H), 7.50 (d, J=8.4 Hz, 1H), 7.25 (d, J=8.4 Hz, 1H), 6.90 (s, 1H), 3.70 (s, 2H), 3.17 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08450307B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-1120329b4621403c85bb2879e360a071
출처 메모uspto-grants-2013_05