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3-(2H-pyran-4(3H,5H,6H)-ylidene)propan-1-ol → 3-(Oxan-4-yl)propan-1-ol

HRID 253577
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HRID 253577 반응식
[O:1]1[CH2:6][CH2:5][C:4](=[CH:7][CH2:8][CH2:9][OH:10])[CH2:3][CH2:2]1>CO.[OH-].[OH-].[Pd+2]>[O:1]1[CH2:6][CH2:5][CH:4]([CH2:7][CH2:8][CH2:9][OH:10])[CH2:3][CH2:2]1
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참가 물질

4

반응물 1

HCID 574196163-(2H-pyran-4(3H,5H,6H)-ylidene)propan-1-ol

생성물 1

HCID 222728913-(Oxan-4-yl)propan-1-ol수율 90%

시약·촉매·용매 2

HCID 9942167Palladium hydroxide촉매HCID 887Methanol용매

실험 절차

To a solution of 3-(2H-pyran-4(3H, 5H, 6H)-ylidene)propan-1-ol (13 g, 0.0916 mol) in methanol (260 mL) was added Pd(OH)2/C (1.3 g). The reaction flask was evacuated and filled with H2. Stirring was continued until the starting material had disappeared. The mixture was filtered through celite, and the filter cake was washed with MeOH (2×10 mL). The combined organic extracts were dried over Na2SO4, and concentrated under vacuum to give the product (11.8 g, 90%), which was used for the next step without purification. 1H NMR (CD3OD) δ 1.1-1.3 (m, 4H), 1.4-1.6 (m, 5H), 2.1-2.3 (s, 1H), 3.3-3.4 (t, 2H), 3.5-3.6 (t, 2H), 3.8-3.9 (dd, 2H).

후처리

  1. customThe reaction flask was evacuated
  2. additionfilled with H2
  3. filtrationThe mixture was filtered through celite
  4. washthe filter cake was washed with MeOH (2×10 mL)
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-c62cbf7aadc14e83b16bc6363ce7c985
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07872028B2

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