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HRID 330680作成日:2026年10月25日

Tert-butyl acetoacetate → tert-Butyl 9,9-bis(2-fluoro-4-methylphenyl)-5-hydroxy-8-(1-methyl-1H-tetrazol-5-yl)-3-oxo-6,8-nonadienoate

https://huagongshe.com/reaction/330680

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl acetoacetateHCID 15538—
反応物5,5-Bis(2-fluoro-4-methylphenyl)-4-(1-methyl-1H-tetrazol-5-yl)-2,4-pentadienalHCID 54207376—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl 9,9-bis(2-fluoro-4-methylphenyl)-5-hydroxy-8-(1-methyl-1H-tetrazol-5-yl)-3-oxo-6,8-nonadienoateHCID 54055970—

反応手順

To a solution of 5,5-bis(2-fluoro-4-methylphenyl)-4-(1-methyl-1H-tetrazol-5-yl)-2,4-pentadienal (1.3 g, 3.4 mmoles) in tetrahydrofuran (15 mL) at -50 ° C. was added the dianion of t-butyl acetoacetate (3.4 mL of a 1M solution, 3.4 mmoles). After stirring for 2 hours, another 0.7 mL of dianion solution was added and the solution stirred for an additional hour. The reaction was quenched with 1N hydrochloric acid and the mixture extracted with methylene chloride. The extracts were dried (MgSO4) and concentrated. The residue was purified by column chromatography on silica gel eluting with 1% (v/v) methanol in methylene chloride to give 1.3 g of the title compound; m.p.=55°-63° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04897490
出典データセットuspto-grants-1990_01
ORD IDord-ed087bbc33d148d4a60f79083939c96e
出典メモuspto-grants-1990_01