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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Triethylamine → HCID 86746895, 화합물

HRID 1586876
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HRID 1586876 반응식
[C:1]([N:9]([CH3:11])[OH:10])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:12]([S:14](Cl)(=[O:16])=[O:15])=[CH2:13].C(N(CC)CC)C>O1CCCC1>[CH:12]([S:14]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[C:1]([N:9]([CH3:11])[OH:10])=[O:8])(=[O:16])=[O:15])=[CH2:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 371715N-hydroxy-N-methylbenzamideHCID 533445Ethenesulfonyl chloride

생성물 1

HCID 86746895HCID 86746895, 화합물수율 76.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

130 ml of tetrahydrofuran was added to a mixture of 7.6 g of N-benzoyl-N-methylhydroxylamine and 6.3 g of vinylsulfonyl chloride and a solution of 5.1 g of triethylamine in 20 ml of tetrahydrofuran was dropwise added to the mixture over 2 hours with stirring while cooling the mixture so that the temperature was maintained at 25° C. or less. The reaction was continued for additional 2 hours at a temperature ranging from 15° to 25° C. and then the same procedures used in Preparation Example 4 were repeated to give 9.2 g of o-vinylsulfonyl N-benzoyl-N-methylhydroxylamine.

후처리

  1. temperaturewhile cooling the mixture so that the temperature
  2. temperaturewas maintained at 25° C. or less
  3. customranging from 15° to 25° C.
  4. customthe same procedures used in Preparation Example 4

출처 및 근거

ORD 기록
ord-a9be31c6d97946c382e1179c89a3dcb7
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05216105

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