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HRID 357657作成日:2026年10月25日

Acetic Acid → Ethyl 4-hydroxy-4-(4-methyl-2-nitrophenyl)-2-butynoate

https://huagongshe.com/reaction/357657

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Ethyl propiolateHCID 12182—
反応物Ammonium ChlorideHCID 25517—
反応物4-Methyl-2-nitrobenzaldehydeHCID 590446—
反応物Lithium diisopropylamideHCID 2724682—
反応物Tetrahydrofuran heptane ethylbenzolHCID 22742125—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 4-hydroxy-4-(4-methyl-2-nitrophenyl)-2-butynoateHCID 1893762298.8%

反応手順

(a-2) To a solution of ethyl propiolate (1.2 ml, 12.0 mmole) in tetrahydrofuran (20 ml) was added at -65° C. under the argon atmosphere a solution of 2.0M lithium diisopropylamide in a mixed solvent of heptane-tetrahydrofuran-ethylbenzene (6.0 ml, 12.0 mole), and the mixture was stirred for 20 minutes. A solution of 4-methyl-2-nitrobenzaldehyde (1.65 g, 10 mmole) in tetrahydrofuran (10 ml) was added, and the reaction mixture was further stirred at 65° C. for 3 hours. To the reaction mixture was added a saturated aqueous ammonium chloride solution (20 ml) or a solution of acetic acid (13.0 ml, 220 mmole) in tetrahydrofuran (20 ml), followed by water, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid, a saturated aqueous sodium hydrogen carbonate solution and a saturated aqueous saline in this sequence, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give ethyl 4-hydroxy-4-(4-methyl-2-nitrophenyl)-2-butynoate as an oil (2.60 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05840895
出典データセットuspto-grants-1998_11
ORD IDord-38e866aa774a4cdc983f18d941234cc0
出典メモuspto-grants-1998_11