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Sodium Hydroxide → Furo[3,2-c]pyridin-6-ylmethanol

HRID 1383003
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HRID 1383003 반응식
[OH2:1].[CH3:2][C:3]1[N+:8]([O-])=[CH:7][C:6]2[CH:10]=[CH:11][O:12][C:5]=2[CH:4]=1.[OH-].[Na+]>C(OC(=O)C)(=O)C.Cl>[OH:1][CH2:2][C:3]1[N:8]=[CH:7][C:6]2[CH:10]=[CH:11][O:12][C:5]=2[CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 21273331HCID 21273331, 화합물

생성물 1

HCID 14005234Furo[3,2-c]pyridin-6-ylmethanol수율 64%

시약·촉매·용매 2

HCID 313Hydrochloric Acid용매HCID 7918Acetic Anhydride용매

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온도
100 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

A mixture of 6-methylfuro[3,2-c]pyridine-N-oxide monohydrate (19.85 g, 0.119 mol) in acetic anhydride (30 mL) was heated at 100° C. for one half hour. Then the reaction mixture was diluted with 20% hydrochloric acid (100 mL) and heating was continued for one hour. The solution was cooled and made basic with sodium hydroxide solution. The product was extracted into chloroform, dried over anhydrous sodium sulfate, filtered through a pad of charcoal and evaporated. The residue was triturated with cool benzene and the crystalline product collected by filtration to give 11.36 g (64% yield), mp: 72°-74° C.

후처리

  1. temperatureheating
  2. temperatureThe solution was cooled
  3. extractionThe product was extracted into chloroform
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered through a pad of charcoal
  6. customevaporated
  7. customThe residue was triturated with cool benzene
  8. filtrationthe crystalline product collected by filtration
  9. customto give 11.36 g (64% yield), mp: 72°-74° C.

출처 및 근거

ORD 기록
ord-a409d72270784fcf98f40e0d728af78f
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04808595

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