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Sodium Chloride → HCID 13037851, 화합물

HRID 434574
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HRID 434574 반응식
P([O-])(O)(O)=O.[K+].[OH-:7].[Na+].[CH3:9][CH:10]([CH:13]([C:15]1[O:16][CH:17]=[CH:18][CH:19]=1)O)[CH:11]=[CH2:12].[Cl-].[Na+]>O>[CH3:9][CH:10]([C:13]1[C:15](=[O:16])[CH2:19][CH:18]([OH:7])[CH:17]=1)[CH:11]=[CH2:12]
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참가 물질

6

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HCID 5234Sodium ChlorideHCID 14798Sodium Hydroxide2회HCID 516951Monobasic potassium phosphateHCID 11788394HCID 11788394, 화합물

생성물 1

HCID 13037851HCID 13037851, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
150 °C

실험 절차

Water (500 ml) and potassium dihydrogenphosphate (2.0 g) were placed in an autoclave, and the mixture was adjusted to pH 5.1 with an aqueous 1N NaOH solution at 30° C. α-Methylallyl-2-furylcarbinol (15 g) was then added, and the mixture was heated at 150° C. for 5.5 hours while stirring. After cooling, the reaction mixture was adjusted to pH 7.1 with an aqueous 1N NaOH solution at 30° C. and re-heated at 150° C. for 5 hours while stirring. After completion of the reaction, the mixture was admixed with sodium chloride (10 g) and extracted with methyl isobutyl ketone. The solvent was removed from the reaction mixture, and distillation of the resulting residue gave 2-(α-methylallyl)-4-hydroxy-2-cyclopentenone with the yield of 12 g (80%). B.P., 88°-90° C./0.12 mmHg.

후처리

  1. additionwas then added
  2. temperatureAfter cooling
  3. temperaturere-heated at 150° C. for 5 hours
  4. stirringwhile stirring
  5. customAfter completion of the reaction
  6. extractionextracted with methyl isobutyl ketone
  7. customThe solvent was removed from the reaction mixture, and distillation of the resulting residue

출처 및 근거

ORD 기록
ord-d075e51516004ebdb9acfb4ebc39aef5
출처 데이터셋
uspto-grants-1983_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04398043

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