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HRID 2383920作成日:2026年10月25日

Acetic Acid → 3-Bromo-4-(pyrrolidin-1-ylmethyl)pyridine

https://huagongshe.com/reaction/2383920

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物PyrrolidineHCID 31268—
反応物3-Bromopyridine-4-carboxaldehydeHCID 2762997—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物3-Bromo-4-(pyrrolidin-1-ylmethyl)pyridineHCID 5963613698.2%

反応手順

Acetic acid (0.1 mL) was added to a stirred solution of 3-bromo-pyridine-4-carbaldehyde (220 mg, 1.18 mmol) and pyrrolidine (0.11 mL, 1.34 mmol) in DCE (15 mL) under nitrogen atmosphere and stirred at room temperature for 2 hours. This was followed by addition of NaBH(OAc)3 (342 mg, 1.612 mmol) at 0° C. over a period of 10 minutes. The resulting reaction mass was stirred for 12 hours at room temperature. The reaction was monitored by TLC (30% ethyl acetate in hexane). The reaction mixture was washed with NaHCO3 solution and extracted using ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to afford 275 mg of the product (98.2% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08263635B2
出典データセットuspto-grants-2012_09
ORD IDord-ba2945e817e84d48a68db6216bdc198c
出典メモuspto-grants-2012_09