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HRID 920855作成日:2026年10月27日

Ethyl diethoxyacetate → HCID 178471714、化合物

https://huagongshe.com/reaction/920855

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl diethoxyacetateHCID 80169—
反応物3'-Chloro-4'-fluoroacetophenoneHCID 520422—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178471714HCID 178471714—

反応手順

To a −78° C. solution of 1-(3-chloro-4-fluorophenyl)ethanone (16.25 g, 94 mmol) and ethyl 2,2-diethoxyacetate (20.73 mL, 113 mmol) in THF (392 mL) was added, dropwise, a solution of LDA (51.8 mL, 104 mmol, 2M in THF). The resultant reaction mixture was gradually allowed to reach room temperature and continued stirring for 16 h. The reaction was carefully quenched with water and diluted with EtOAc. The two layers were separated and the aq. layer was extracted with EtOAc (2×150 mL) The combined organic layer was washed with brine, dried over anhydrous MgSO4, filtered and the filtrate was concentrated under reduced pressure to provide a crude oil. It was purified by silica gel chromatography (1500 g Commodity column, eluting with a 10% EtOAc in hexanes). Fractions containing the product were combined and evaporated to afford Intermediate A39A (9.97 g, 35%) as a solid. MS(ES): m/z=257 [M-OEt]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09273058B2
出典データセットuspto-grants-2016_03
ORD IDord-64868f37ea864363897c8a57e044ad9c
出典メモuspto-grants-2016_03