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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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O-Methylhydroxylamine → HCID 178526360, 화합물

HRID 1362900
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HRID 1362900 반응식
[Cl:1][C:2]1[N:7]=[N:6][C:5](/[N:8]=[C:9](\Cl)/[C:10]([F:13])([F:12])[F:11])=[CH:4][CH:3]=1.C[O:16][NH2:17]>O1CCCC1>[Cl:1][C:2]1[N:7]=[N:6][C:5]([NH:8]/[C:9](=[N:17]\[OH:16])/[C:10]([F:13])([F:12])[F:11])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 4113O-MethylhydroxylamineHCID 178506325HCID 178506325, 화합물

생성물 1

HCID 178526360HCID 178526360, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 4.5 g (18 mmol) of the crude product of Step B in 150 mL tetrahydrofuran was carefully added 2 mL aqueous 50% methoxyamine. The resulting solution was stirred under nitrogen at ambient temperature. After 1 h the solution was concentrated in vacuo then dissolved in 100 mL ethyl acetate and washed sequentially with saturated aqueous sodium bicarbonate solution and saturated aqueous brine (100 mL each). The organic phase was then dried over magnesium sulfate, filtered, and evaporated in vacuo to yield a crude oil.

후처리

  1. concentrationAfter 1 h the solution was concentrated in vacuo
  2. dissolutionthen dissolved in 100 mL ethyl acetate
  3. washwashed sequentially with saturated aqueous sodium bicarbonate solution and saturated aqueous brine (100 mL each)
  4. dry with materialThe organic phase was then dried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customto yield a crude oil

출처 및 근거

ORD 기록
ord-c1bed97882614b2bae1281e85b833931
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07884104B2

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