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Methanol → HCID 15340226, 화합물

HRID 1734764
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HRID 1734764 반응식
[CH2:1]([C:3]1([CH2:10][O:11][C:12](=[O:16])[C:13]([CH3:15])=[CH2:14])[CH2:8][O:7][C:6](=[O:9])[O:5][CH2:4]1)[CH3:2].[CH3:17][OH:18].C1(C)C=CC(S(O)(=O)=O)=CC=1>ClCCCl>[CH2:1]([C:3]([CH2:10][O:11][C:12](=[O:16])[C:13]([CH3:15])=[CH2:14])([CH2:8][O:7][C:6]([O:5][CH3:4])=[O:9])[CH2:17][OH:18])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 6101p-Toluenesulfonic acidHCID 15340225(5-Ethyl-2-oxo-1,3-dioxan-5-yl)methyl 2-methylprop-2-enoate

생성물 1

HCID 15340226HCID 15340226, 화합물

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

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온도
40 °C

실험 절차

11.4 g of 5-ethyl-5-methacryloyloxymethyl-2-oxo-1,3-dioxane, 3.2 g of methanol and 0.285 g of p-toluenesulfonic acid were dissolved in 100 g of 1,2-dichloroethane. The solution was stirred for 2 hours at 40° C. and evaporated in vacuo to remove the solvent. After removing white precipitates by filtration, the residue was further concentrated whereupon the title compound was recovered as a colorless oil.

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후처리

  1. customevaporated in vacuo
  2. customto remove the solvent
  3. customAfter removing white
  4. customprecipitates by filtration
  5. concentrationthe residue was further concentrated whereupon the title compound
  6. customwas recovered as a colorless oil

출처 및 근거

ORD 기록
ord-212fb9b2def342a8a5ac3dba886a813d
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05534647

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