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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → HCID 11264379, 화합물

HRID 459544
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HRID 459544 반응식
C([O:3][C:4]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][N+:13]=2[O-:18])=[CH:8][CH:7]=1)=[O:5])C.N1C=CC=CC=1C1C=CC(C(O)=O)=CC=1.[OH-].[Na+]>O1CCOCC1>[C:4]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][N+:13]=2[O-:18])=[CH:8][CH:7]=1)([OH:5])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 8216924-(2-Pyridyl)Benzoic AcidHCID 147974372-(4-Ethoxycarbonylphenyl)pyridine N-oxide

생성물 1

HCID 11264379HCID 11264379, 화합물수율 87.8%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

2-(4-Ethoxycarbonylphenyl)pyridine N-oxide (260 mg) synthesized from 4-(2-pyridyl)benzoic acid in the same manner as in the above Referetnial Example was dissolved in 1,4-dioxane (10 ml), a 1N aqueous solution (2.00 ml) of sodium hydroxide was added, and the mixture was heated under reflux for 2 hours. The reaction mixture was concentrated under reduced pressure, 1N hydrochloric acid (6 ml) was added to the residue, and precipitate formed was collected by filtration to obtain the title compound (202 mg) as a colorless amorphous solid.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 2 hours
  3. concentrationThe reaction mixture was concentrated under reduced pressure, 1N hydrochloric acid (6 ml)
  4. additionwas added to the residue, and precipitate
  5. customformed
  6. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-69b82c8bb6bf4ac3a58f6170c974301a
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07192968B2

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