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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Anhydride → N-(3-Iodo-2-methylphenyl)acetamide

HRID 1185981
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HRID 1185981 반응식
[I:1][C:2]1[C:3]([CH3:9])=[C:4]([CH:6]=[CH:7][CH:8]=1)[NH2:5].[C:10](OC(=O)C)(=[O:12])[CH3:11]>C(O)(=O)C>[C:10]([NH:5][C:4]1[CH:6]=[CH:7][CH:8]=[C:2]([I:1])[C:3]=1[CH3:9])(=[O:12])[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 189261443-Iodo-2-methylaniline

생성물 1

HCID 25138592N-(3-Iodo-2-methylphenyl)acetamide

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Charge a 5 L, 3 neck flask equipped with a mantle, stirrer, condenser, with 708 grams (5M) 3-Iodo-2-Methyl Aniline, followed by 700 ml glacial acetic acid. Add in a stream of 520 grams (5.1M) acetic anhydride and allow the solution to come to a gentle reflux for an hour. The solution is allowed to cool and poured in a stream in a large container of 8 L ice water. The product will crystallize immediately and is filtered and squeezed under vacuum and air-dried. Yield was 900 grams (Theoretical yield=918 g).

후처리

  1. additionCharge a 5 L, 3 neck flask
  2. customequipped with a mantle, stirrer, condenser
  3. temperaturea gentle reflux for an hour
  4. temperatureto cool
  5. customThe product will crystallize immediately
  6. filtrationis filtered
  7. customair-dried

출처 및 근거

ORD 기록
ord-16cceccfd18c4d05bcbde8bb252c462d
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08673269B2

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