돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662223생성일: 2026년 10월 23일

m-Anisoyl chloride → 4-Chloro-2-fluoro-6-(3-methoxybenzoyl)benzonitrile

https://huagongshe.com/ko/reaction/1662223

반응식

참여 물질

역할이름HCID투입량
반응물m-Anisoyl chlorideHCID 74374—
반응물Lithium BromideHCID 82050—
반응물2-Bromo-4-chloro-6-fluorobenzonitrileHCID 58579537—
반응물HCID 178418546HCID 178418546—
촉매ZincHCID 23994—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-2-fluoro-6-(3-methoxybenzoyl)benzonitrileHCID 5857952455%

반응 단계

2-Bromo-4-chloro-6-fluorobenzonitrile (6.95 g, 29.64 mmol) was dissolved in THF (15 mL) and added to a bottle of Rieke® Zinc in THF (50 mg/mL, 50.0 mL, 38.24 mmol) at 0° C. under an argon atmosphere. The resulting mixture was stirred at rt for 6 h and then stored in a refrigerator for 60 h allowing the excess of zinc to settle. The solution was carefully decanted off and cooled to −78° C. under an argon atmosphere. A solution of lithium bromide (5.15 g, 59.28 mmol) and copper(I) cyanide (2.65 g, 29.64 mmol) in THF (30 mL) was added and the resulting mixture was stirred at rt for 30 min. The mixture was cooled to −78° C. and then 3-methoxybenzoyl chloride (4.17 mL, 29.64 mmol) was added dropwise. The cooling bath was removed and the resulting mixture was stirred at rt for 1.5 h. Saturated aqueous NH4Cl (12 mL) was added to the mixture, the THF was removed in vacuo and the residue was diluted with water (50 mL) and DCM (50 mL). The mixture was poured into a phase separator, the organic phase was collected, concentrated and purified on a silica gel column (0-30% EtOAc in heptane) to give 4.7 g (55%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030500B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-e6852b5321c84dbb9f7c3449ee6208b3
출처 메모uspto-grants-2011_10