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HRID 1362031作成日:2026年10月27日

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

https://huagongshe.com/reaction/1362031

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物3-Chloro-1-benzothiophene-2-carbaldehydeHCID 818121—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物(3-Chlorobenzo[b]thiophen-2-ylmethyl)methylamineHCID 642481880%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07879872B2
出典データセットuspto-grants-2011_02
ORD IDord-78bf07c8b1644ba693b8b4cf939c9737
出典メモuspto-grants-2011_02