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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362031생성일: 2026년 10월 26일

Methylamine → (3-Chlorobenzo[b]thiophen-2-ylmethyl)methylamine

https://huagongshe.com/reaction/1362031

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물3-Chloro-1-benzothiophene-2-carbaldehydeHCID 818121—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
생성물(3-Chlorobenzo[b]thiophen-2-ylmethyl)methylamineHCID 642481880%

반응 단계

To 3-chloro-benzo[b]thiophene-2-carbaldehyde (1.9 g, 9.5 mmol) was added a solution of 2 M methylamine in methanol (32 mL) and the resulting mixture was stirred overnight at room temperature. The mixture was concentrated under reduced pressure and the residue taken up in ethanol (32 mL). The solution was cooled to 0° C., NaBH4 (0.54 g, 14 mmol) was added in one portion and stirring continued overnight. The mixture was concentrated under reduced pressure and the residue solvated in 1 M NaOH (200 mL). The mixture was extracted with diethyl ether (3×150 mL) and the combined organics were washed with brine (100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to give a yellow oil. Purification by flash column chromatography (silica gel, hexanes/ethyl acetate 1:1) gave the title compound (1.62 g, 80%) as a pale yellow oil which crystallized under vacuum: 1H NMR (300 MHz, CDCl3) δ 7.70 (m, 2H), 7.45 (m, 2H), 4.08 (s, 2H), 2.51 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879872B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-78bf07c8b1644ba693b8b4cf939c9737
출처 메모uspto-grants-2011_02