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HRID 375555作成日:2026年10月25日

2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- → 1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclohexane

https://huagongshe.com/reaction/375555

反応式

関与物質

役割名称HCID仕込み量
反応物2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
反応物1-Chloro-5-iodopentaneHCID 108914—
反応物1-(Carboethoxy)-1-(4-methoxybenzylthio)methaneHCID 10847644—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclohexaneHCID 2240021356.6%

反応条件

温度-78 °C

反応手順

Cool lithium hexamethyldisilazane (8.4 mL of a 1.0M solution in tetrahydrofuran, 8.4 mmol) to -78° C. Add , by cannula transfer, a solution of 1-(carboethoxy)-1-(4-methoxybenzylthio)methane (2.0 g, 8.3 mmol) in tetrahydrofuran (8 mL). Stir for 45 minutes then add a solution of 1-iodo-5-chloropentane (1.94 g, 8.32 mmol) in tetrahydrofuran (8 mL). Stir for 1 hour and add 1,3-dimethyl-3,4,5, 6-tetrahydro -2(1H)-pyrimidinone (DMPU) (1.21 mL, 10.0 mmol). Stir at 0° C. for 4 hours and at room temperature for 6 hours. Cool to -78° C., add lithium hexamethyldisilazane (8.4 mL, 8.4mmol) and stir at room temperature overnight. Quench with saturated ammonium chloride (5 mL) and partition between ethyl acetate (50 mL) and water (50 mL). Separate the organic phase, dry (Na2SO4) and evaporate the solvent in vacuo. Purify by chromatography (6:1 hexane/ethyl acetate) to give 1-(carboethoxy)-1-(4-methoxybenzylthio)cyclohexane as an colorless oil (1.45 g, 56%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05486513
出典データセットuspto-grants-1996_01
ORD IDord-0958d114d8864b7a8c2a5245205c059d
出典メモuspto-grants-1996_01