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HRID 260693作成日:2026年10月26日

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

https://huagongshe.com/reaction/260693

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, 8.4 mmol) 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US05529996
出典データセットuspto-grants-1996_06
ORD IDord-be75b6e3c31c4b169e917fe29e3a3ac3
出典メモuspto-grants-1996_06