Hydrochloric Acid → 4-Benzhydrylpyridine

HRID 1193636

반응식

HRID 1193636 반응식
[C:1]1([C:7]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)([C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.I.[OH-].[Na+].S([O-])([O-])(=O)=S.[Na+].[Na+]>C(O)(=O)C>[C:1]1([CH:7]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:9]2[CH:10]=[CH:11][N:12]=[CH:13][CH:14]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 24477Sodium ThiosulfateHCID 24841Hydrogen iodideHCID 74177alpha,alpha-Diphenyl-4-pyridinemethanol

생성물 1

HCID 772524-Benzhydrylpyridine

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 99 g (0.379 mole) of diphenyl-4-pyridyl-methanol, 50 ml of conc. hydrochloric acid, 200 ml of 57% hydroiodic acid and 200 ml of glacial acetic acid was refluxed for 41/2 hr and then was stirred at room temperature for 12 hr. The reaction mixture was poured over ice and was made basic with 50% sodium hydroxide. An aqueous solution of sodium thiosulfate was added, and the mixture was extracted with methylene chloride. The methylene chloride solution was dried over magnesium sulfate and the solvent was removed in vacuo. The residue was recrystallized from a mixture of methylene chloride-ether-hexane to give two crops of crystalline solids: Crop I, 40.87 g (44.0%), m.p. 124-126; Crop II, 25.38 g (27.3%), m.p. 123-125. Analysis of the mixture of the Crops I and II was as follows:

후처리

  1. temperaturewas refluxed for 41/2 hr
  2. additionThe reaction mixture was poured over ice
  3. extractionthe mixture was extracted with methylene chloride
  4. dry with materialThe methylene chloride solution was dried over magnesium sulfate
  5. customthe solvent was removed in vacuo
  6. customThe residue was recrystallized from a mixture of methylene chloride-ether-hexane
  7. customto give two crops of crystalline solids

출처 및 근거

ORD 기록
ord-f0394fceb32449ae8535dcd4e97b96bd
출처 데이터셋
uspto-grants-1989_03
특허 번호
US04810713

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