돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374953생성일: 2026년 10월 26일

Dimethylformamide → 2,3-Dichloro-6-fluorobenzaldehyde

https://huagongshe.com/reaction/374953

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물CyclohexaneHCID 8078—
반응물1,2-Dichloro-4-fluorobenzeneHCID 74028—
반응물Acetone cardiceHCID 18522661—
반응물CID 53628100HCID 178418400—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2,3-Dichloro-6-fluorobenzaldehydeHCID 3260062—

반응 조건

온도-45 °C

반응 단계

A solution of 1.3M s-butyl lithium in cyclohexane (244 mL, 317 mmol) is added to a dry-ice/acetone cooled solution of TMEDA (34 g, 293 mmol) in THF (250 mL), maintaining the internal reaction temperature <-70° C. The resulting reaction mixture is cooled and maintained at ≤-90° C. with an ether/liquid nitrogen bath while a solution of 1,2-dichloro-4-fluorobenzene (40 g, 244 mmol) in THF (100 mL) is added dropwise. The resulting reaction mixture is stirred with dry-ice/acetone cooling for 1h, then is cannulated into an ether/liquid nitrogen cooled and mechanically stirred solution of DMF (89.1 g, 1.22 mol) in THF (125 mL). The resulting mixture is warmed to -45° C. and partitioned between dilute aqueous HCl and ether. The organic solution is washed with aqueous NaHCO3, dried (MgSO4), and concentrated to afford 44.38 g of 2-fluoro-5,6-dichlorobenzaldehyde as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05482974
출처 데이터셋uspto-grants-1996_01
ORD IDord-c71469b9738f4ef7aae2f3a53f0962d6
출처 메모uspto-grants-1996_01