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HRID 1662223作成日:2026年10月25日

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

https://huagongshe.com/reaction/1662223

反応式

関与物質

役割名称HCID仕込み量
反応物m-Anisoyl chlorideHCID 74374—
反応物Lithium BromideHCID 82050—
反応物2-Bromo-4-chloro-6-fluorobenzonitrileHCID 58579537—
反応物HCID 178418546HCID 178418546—
触媒ZincHCID 23994—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-2-fluoro-6-(3-methoxybenzoyl)benzonitrileHCID 5857952455%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030500B2
出典データセットuspto-grants-2011_10
ORD IDord-e6852b5321c84dbb9f7c3449ee6208b3
出典メモuspto-grants-2011_10