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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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m-Chloroperbenzoic acid → HCID 19010447, 화합물

HRID 1741591
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HRID 1741591 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[F:12][C:13]1[CH:14]=[C:15]([CH:23]=[CH:24][CH:25]=1)[O:16][C:17]1[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=1.S([O-])(O)=O.[Na+]>C(Cl)Cl>[F:12][C:13]1[CH:14]=[C:15]([CH:23]=[CH:24][CH:25]=1)[O:16][C:17]1[CH:18]=[N+:19]([O-:9])[CH:20]=[CH:21][CH:22]=1
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참가 물질

5

반응물 3

HCID 70297m-Chloroperbenzoic acidHCID 126734843-(3-Fluorophenoxy)pyridineHCID 23665763Sodium Bisulfite

생성물 1

HCID 19010447HCID 19010447, 화합물수율 85%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 46.3 g of m-chloroperbenzoic acid in 460 ml of methylene chloride, 37.35 g of 3-(3-fluorophenoxy)pyridine was added at room temperature, and the mixture was stirred at room temperature for 1.5 hours. An aqueous sodium hydrogen sulfite solution (20%, 120 ml) was added to the mixture and then the mixture was stirred for a few minutes. The organic layer separated was washed with 10% aqueous sodium hydroxide solution and with water, dried over anhydrous sodium sulfate, and concentrated. The residue was crystallized by trituration with isopropyl ether. The crystals were collected by filtration and washed with isopropyl ether to yield 34.44 g of pale yellow crystals, which were recrystallized from ethyl acetate to give colorless needles, mp 59°-61° C.

후처리

  1. stirringthe mixture was stirred for a few minutes
  2. customThe organic layer separated
  3. washwas washed with 10% aqueous sodium hydroxide solution and with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customThe residue was crystallized by trituration with isopropyl ether
  7. filtrationThe crystals were collected by filtration
  8. washwashed with isopropyl ether

출처 및 근거

ORD 기록
ord-d0d03700173f4b0e977ff52aae7f3d10
출처 데이터셋
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05334594

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