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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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p-Toluenesulfonic acid → HCID 19973607, 화합물

HRID 2398090
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인쇄 미리보기

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HRID 2398090 반응식
C(O)CCO.C(C=C)=O.[C:10]1([CH3:20])[CH:15]=CC(S(O)(=O)=O)=C[CH:11]=1.[CH:21]([CH:23]1[O:28]CCC[O:24]1)=[CH2:22]>O>[CH:21]([CH:23]1[O:28][CH2:11][CH:10]([CH3:20])[CH2:15][O:24]1)=[CH2:22]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6101p-Toluenesulfonic acidHCID 7847Acrolein3회HCID 104421,3-PropanediolHCID 800432-Vinyl-1,3-dioxane2회

생성물 1

HCID 19973607HCID 19973607, 화합물

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
26 °C

실험 절차

For the sake of comparison, a mixture of 0.5 mole 1,3-propanediol and 0.55 mole acrolein were reacted at 50° C in the presence of 0.3 g. p-toluenesulfonic acid. Layers did not separate until the reaction mixture was cooled to 26° C. The mixture gave 18 g. of an aqueous layer which contained about 40% diol, 21% acrolein, 10% 2-vinyl-1,3-dioxane and 25% water. The acetal layer of 49 g. contained 63% 2-vinyl-1,3-dioxane, 23% acrolein, 8% diol and 5% water, conversion to acetal was about 60% which represents only a negligible increase over equilibrium conversion.

후처리

  1. customwere reacted at 50° C in the presence of 0.3 g
  2. customLayers did not separate until the reaction mixture
  3. customThe mixture gave 18 g
  4. temperaturea negligible increase over equilibrium conversion

출처 및 근거

ORD 기록
ord-1089ba5253cf43a1abaa83aa753ace14
출처 데이터셋
uspto-grants-1977_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04024159

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