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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362411생성일: 2026년 10월 25일

Water → Benzo[b]thiophene-5-methanamine, N-methyl-

https://huagongshe.com/reaction/1362411

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물MethylamineHCID 6329—
반응물Benzo(b)thiophene-5-carboxaldehydeHCID 139097—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물Benzo[b]thiophene-5-methanamine, N-methyl-HCID 1664060789.3%

반응 단계

Benzo[b]thiophene-5-carbaldehyde (276 mg, 1.70 mmol) was dissolved in anhydrous methanol (8.0 mL). Methylamine (0.68 mL of 33% solution in ethanol, 5.46 mmol) was added and the reaction was stirred for 3 h. The solution was concentrated to a white solid and then dissolved in anhydrous methanol (10 mL). Sodium borohydride (66.0 mg, 1.75 mmol) was added and the mixture was stirred overnight at room temperature. Water (8.0 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 benzo[b]thiophen-5-yl-N-methylmethanamine (269 mg, 89%) as a yellow oil: 1H NMR (300 MHz, DMSO-d6) δ 7.90 (d, J=8.7 Hz, 1H), 7.79 (s, 1H), 7.71 (d, J=5.7 Hz, 1H), 7.40 (d, J=5.4 Hz, 1H), 7.32 (d, J=8.1 Hz, 1H), 3.73 (s, 2H), 2.26 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-01bdf37b587d44d88ea35b8b2a352470
출처 메모uspto-grants-2011_02