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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1093929생성일: 2026년 10월 27일

Iodine → 3,4-Dihydro-2h-pyran-2-ylmethyl acetate

https://huagongshe.com/reaction/1093929

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물PyridineHCID 1049—
반응물Acetic AnhydrideHCID 7918—
반응물3,4-dihydro-2H-pyran-2-methanolHCID 95559—
용매Ethyl AcetateHCID 8857—
생성물3,4-Dihydro-2h-pyran-2-ylmethyl acetateHCID 22812686%

반응 조건

온도0 °C

반응 단계

A mixture of (±)-3,4-dihydro-2H-pyran-2-methanol (514 g, 4.51 mol, 1 eq) and acetic anhydride (621 g, 6.09 mol, 1.35 eq) was cooled to 0° C. To the resultant mixture was added pyridine (35.6 g, 0.45 mol, 0.1 eq) and the resultant reaction mixture was allowed to warm to room temperature with stirring. The resultant reaction mixture was allowed to stir for an additional 8 hours after reaching room temperature and was shown to be complete by thin-layer chromatography (2:1 hexanes:ethyl acetate, I2 staining). The reaction mixture was concentrated in vacuo at 35° C. and the resultant residue was diluted using ethyl acetate (2 L). The resultant mixture was transferred to a separatory funnel and sequentially washed with deionized water (3×1 L), saturated aqueous NaHCO3 (2×10 L), and brine (1.0 L). The organic layer was dried over sodium sulfate and concentrated in vacuo at 35° C. to provide (±)-3,4-dihydro-2H-pyran-2-yl-methyl acetate as a clear liquid (605.9 g, 86% yield). 1H NMR (300 MHz, CDCl3) δ 1.6-2.2 (m, 4H), 2.1 (s, 3H), 4.2 (m, 3H), 4.8 (m, 1H), 6.4 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08133880B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-d5beb6b512e84af88224305ee09a2175
출처 메모uspto-grants-2012_03