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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Nitric Acid → 3-Bromo-2-nitrothiophene

HRID 1370191
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HRID 1370191 반응식
[N+:1]([O-:4])(O)=[O:2].C(OC(=O)C)(=O)C.[Br:12][C:13]1[CH:17]=[CH:16][S:15][CH:14]=1>C(O)(=O)C>[Br:12][C:13]1[CH:17]=[CH:16][S:15][C:14]=1[N+:1]([O-:4])=[O:2]
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참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 7918Acetic AnhydrideHCID 133833-Bromothiophene

생성물 1

HCID 12014963-Bromo-2-nitrothiophene

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

7.4 ml of fuming nitric acid was slowly added to 92.1 ml of acetic acid under ice-cooling, followed by stirring for 10 minutes, and a solution of 52.1 ml of acetic anhydride containing 25 g of 3-bromothiophene was slowly added in such a manner that the bulk temperature did not exceed 10° C., followed by stirring at 10 ° C. for 2 hours. Ice was added to the reaction solution, and the resulting crystals were collected by filtration, and washed with water and diethyl ether/n-hexane=1/5 successively, to give 17.4 g of the title compound.

후처리

  1. temperaturecooling
  2. customdid not exceed 10° C.
  3. stirringby stirring at 10 ° C. for 2 hours
  4. additionIce was added to the reaction solution
  5. filtrationthe resulting crystals were collected by filtration
  6. washwashed with water and diethyl ether/n-hexane=1/5 successively

출처 및 근거

ORD 기록
ord-4f032b09762d403b9ad74e2a78a53d80
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06583138B1

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