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HRID 460021作成日:2026年10月23日

2-Methylbenzenesulfonic acid → HCID 69522022、化合物

https://huagongshe.com/ja/reaction/460021

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylbenzenesulfonic acidHCID 6925—
反応物Lithium diisopropylamideHCID 2724682—
反応物4-Methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carbaldehydeHCID 2782899—
反応物56443-69-7HCID 12969325—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 69522022HCID 69522022—

反応条件

温度0 °C

反応手順

A mixture of 1-[4-(benzyloxy)-3-methylphenyl]ethanone (intermediate 8, 1.15 g) in dry tetrahydrofuran (15 ml) at −78° C. was treated dropwise with lithium diisopropylamide (2.6 ml of 2M solution in heptane/tetrahydrofuran/ethylbenzene) under nitrogen. The reaction mixture was warmed to 0° C. for 30 minutes. The mixture was cooled to −78° C. and 4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-5-carbaldehyde (intermediate 2, 1.08 g) in dry tetrahydrofuran (15 ml) was added drop-wise at −78° C. and the reaction mixture stirred at 21° C. for 2 hours. Acetic acid (4 ml) in dry tetrahydrofuran (4 ml) was added followed by toluenesulphonic acid (0.1 g) and the reaction mixture was heated at 50° C. for 1 hour and then concentrated. The residue was partitioned between saturated bicarbonate solution and ethyl acetate; the aqueous layer separated and extracted thrice more with ethyl acetate. The organic solutions were combined and were dried with brine and over magnesium sulfate and concentrated. The product isolated after evaporation of the solvent was further purified by flash chromatography using cyclohexane:ethyl acetate (6:1) as eluent to give the title compound as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196107B2
出典データセットuspto-grants-2007_03
ORD IDord-1cee6bc02cd2484b9ffb34dbfe215a32
出典メモuspto-grants-2007_03