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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375555생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/375555

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참여 물질

역할이름HCID투입량
반응물2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
반응물1-Chloro-5-iodopentaneHCID 108914—
반응물1-(Carboethoxy)-1-(4-methoxybenzylthio)methaneHCID 10847644—
반응물Lithium bis(trimethylsilyl)amideHCID 57426343—
용매TetrahydrofuranHCID 8028—
생성물1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclohexaneHCID 2240021356.6%

반응 조건

온도-78 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05486513
출처 데이터셋uspto-grants-1996_01
ORD IDord-0958d114d8864b7a8c2a5245205c059d
출처 메모uspto-grants-1996_01