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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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O-Methylhydroxylamine hydrochloride → HCID 86093123, 화합물

HRID 1294708
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인쇄 미리보기

반응식

HRID 1294708 반응식
[N:1]1([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[C:13](=O)[CH3:14])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.Cl.[CH3:17][O:18][NH2:19]>N1C=CC=CC=1.C(OCC)(=O)C>[CH3:17][O:18][N:19]=[C:13]([C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[N:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1)[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 521874O-Methylhydroxylamine hydrochlorideHCID 142678081-(2-(Morpholin-4-yl)phenyl)ethan-1-one

생성물 1

HCID 86093123HCID 86093123, 화합물수율 93.4%

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of Example 49A (1.22 g, 5.94 mmol) and methoxyamine hydrochloride (550 mg, 6.59 mmol) in pyridine (20 mL) was stirred at room temperature for 12 h. The reaction was diluted with ethyl acetate and washed sequentially with 3 N HCl, 1 N HCl and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure to give 1.3 g of the title compound. MS (ESI+) m/z 235 (M+H)+.

후처리

  1. washwashed sequentially with 3 N HCl, 1 N HCl and brine
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-c8ba335ca5ed4a5ba5d22c9fd6b9ecaa
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241776B2

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