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Dimethyl 2,2'-(1,3-dioxolane-2,2-diyl)diacetate → 2-(2-(2-Hydroxyethyl)-1,3-dioxolan-2-yl)ethan-1-ol

HRID 1809845
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HRID 1809845 반응식
[O:1]1[CH2:5][CH2:4][O:3][C:2]1([CH2:11][C:12](OC)=[O:13])[CH2:6][C:7](OC)=[O:8].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[O:1]1[CH2:5][CH2:4][O:3][C:2]1([CH2:6][CH2:7][OH:8])[CH2:11][CH2:12][OH:13]
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참가 물질

4

반응물 2

HCID 228900Dimethyl 2,2'-(1,3-dioxolane-2,2-diyl)diacetateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 5760202-(2-(2-Hydroxyethyl)-1,3-dioxolan-2-yl)ethan-1-ol수율 66.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 2.6 g (12 mmol) of dimethyl 2,2′-(1,3-dioxolane-2,2-diyl)diacetate in 100 mL of dry THF was added 1.4 g (36 mmol) of LAH at 0° C. The reaction mixture was then refluxed for 1 h, was quenched with 15% NaOH aqueous solution (3 mL) and water (3 mL). The mixture was stirred overnight, filtered through celite. The residue was washed twice with THF (100 mL×2). The combined organic phase was evaporated. Chromatography on silica gel afforded 1.3 g (8.0 mmol, yield: 66%) of 2,2′-(1,3-dioxolane-2,2-diyl)diethanol: MS (m/e): 163 (M+1)+.

후처리

  1. temperatureThe reaction mixture was then refluxed for 1 h
  2. customwas quenched with 15% NaOH aqueous solution (3 mL) and water (3 mL)
  3. filtrationfiltered through celite
  4. washThe residue was washed twice with THF (100 mL×2)
  5. customThe combined organic phase was evaporated

출처 및 근거

ORD 기록
ord-14f06a0977364f31a6b4e2d539cc14a3
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08362003B2

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