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Ethylene Glycol → 2-Indanyl-4-methyl-1,3-dioxolane

HRID 278846
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HRID 278846 반응식
[CH:1]1([CH:10]=[O:11])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.C1C2C(=CC=CC=2)C[CH:13]1[CH:21]=[O:22].[CH2:23](O)CO>C1(C)C=CC(S(O)(=O)=O)=CC=1.C1(C)C=CC=CC=1>[CH:1]1([CH:10]2[O:22][CH:21]([CH3:13])[CH2:23][O:11]2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 174Ethylene GlycolHCID 111161982,3-dihydro-1H-indene-1-carbaldehydeHCID 117447712,3-Dihydro-1H-indene-2-carbaldehyde

생성물 1

HCID 113216642-Indanyl-4-methyl-1,3-dioxolane

시약·촉매·용매 2

HCID 6101p-Toluenesulfonic acid촉매HCID 1140Toluene용매
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실험 절차

A solution of 297 grams of a mixture of 70% Indancarbaldehyde and 30% indan-2-carbaldehyde, 300 grams of ethylene glycol, 6 grams of p-toluenesulfonic acid and 300 grams of toluene are heated 2 hours at reflux using a Dean-Stark trap to separate water. The mixture is cooled and washed with 200 milliliters of a 5 weight % sodium carbonate solution. The organic layer is distilled to provide 321 grams of 2-indanyl-4-methyl-1,3-dioxolane (b.p.121° C. at 3 mm).

후처리

  1. temperatureat reflux
  2. customto separate water
  3. temperatureThe mixture is cooled
  4. washwashed with 200 milliliters of a 5 weight % sodium carbonate solution
  5. distillationThe organic layer is distilled

출처 및 근거

ORD 기록
ord-0e698486875c4deca9c33f8d8703e1f3
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06362141B1

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