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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 237861생성일: 2026년 10월 26일

Iodoethane → Methyl acetate hexane

https://huagongshe.com/reaction/237861

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Sodium hydrideHCID 24758—
반응물4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-olHCID 11123315—
용매DimethylformamideHCID 6228—
생성물Methyl acetate hexaneHCID 234493021%
생성물2-(4-Ethoxy-but-2-ynyloxy)-tetrahydro-pyranHCID 68529463—

반응 조건

온도0 °C

반응 단계

An oven dried 500 ml RBF was charged with NaH (60% in mineral oil) (1.41 g, 35.3 mmol) and suspended in DMF (100 mL). The mixture was cooled to 0° C. and 4-(tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol (prepared in accordance with the procedures of Tamaru et al., Bull. Chem. Soc. Jpn., 1995, 1689-1705) (6.0 g, 35.3 mmol) was added. The reaction mixture was allowed to reach room temperature and stirred for one hour. To the mixture was added iodoethane (20.8 g, 133 mmol). The reaction mixture was stirred for 3.5 hours at room temperature before being quenched with ice/H2O and extracted with MeOAc. The organic phase was washed with brine, dried (Na2SO4) and concentrated. Silica gel chromatography (1-20% MeOAc/hexane) provided 4.71 g of 2-(4-ethoxy-but-2-ynyloxy)-tetrahydro-pyran as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642603B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-fd436759d4e74f2f98770a0ccab266a0
출처 메모uspto-grants-2014_02