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HRID 7001作成日:2026年10月25日

Dimethylformamide → 3-Bromo-5-fluorobenzaldehyde

https://huagongshe.com/reaction/7001

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1,3-Dibromo-5-fluorobenzeneHCID 137003—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物3-Bromo-5-fluorobenzaldehydeHCID 21986246100%

反応手順

To a solution of 3,5-dibromofluorobenzene in diethyl ether (100 cm3) at −78° C. was added n-butyl lithium (2.5 M, 8 cm3, 20 mmol) dropwise. After 30 min. the mixture was treated with DMF (20 cm3) in diethyl ether (10 cm3) and stirring was continued at −78° C. After 30 min. the mixture was quenched with dilute HCl aq., separated and the aqueous layer was extracted with EtOAc. The combined organic layers were combined, washed with water, brine, dried (MgSO4) and evaporated to give 3-fluoro-5-bromobenzaldehyde (4.0 g, 19.7 mmol, 100%) as an oil: 1H NMR (CDCl3) δ inter alia 7.50–7.53 (m, 2H), 7.82 (s, 1H) and 9.93 (m, 1H); MS (EI) m/z 202, 204 [M+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084168B2
出典データセットuspto-grants-2006_08
ORD IDord-9ecd93464dc648fe987299a1452499ec
出典メモuspto-grants-2006_08