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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Formic Acid → HCID 15580713, 화합물

HRID 1702643
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HRID 1702643 반응식
[CH:1](O)=O.Cl[C:5]1[CH:6]=[C:7]([N:12]2[CH2:16][CH:15](C)[C:14]([NH:18][CH:19]=[O:20])=[N:13]2)[CH:8]=[CH:9][C:10]=1[Cl:11].CCCCCC>ClCCl>[Cl:11][C:10]1[CH:5]=[CH:6][C:7]([N:12]2[CH:16]([CH3:1])[CH2:15][C:14]([NH:18][CH:19]=[O:20])=[N:13]2)=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 284Formic AcidHCID 8058HexaneHCID 15580721HCID 15580721, 화합물

생성물 1

HCID 15580713HCID 15580713, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A 4.8 g. amount of the above compound is dissolved in 25.0 ml. of a mixture of formic acid and acetic anhydride (Example 15). The reaction mixture is allowed to remain at room temperature for 3 hours, then ice water is added to separate a gum. The aqueous phase is decanted and the gum is dissolved in dichloromethane. The solution is dried over magnesium sulfate and passed through a hydrous magnesium silicate. The effluent is evaporated leaving a gum. The gum is dissolved in dichloromethane. The solution is heated and hexane is added until turbidity results. The mixture is cooled and filtered to yield 3.6 g. of the desired product as off-white crystals, m.p. 112°-113° C.

후처리

  1. dissolutionamount of the above compound is dissolved in 25.0 ml
  2. customto separate a gum
  3. customThe aqueous phase is decanted
  4. dissolutionthe gum is dissolved in dichloromethane
  5. dry with materialThe solution is dried over magnesium sulfate
  6. customThe effluent is evaporated
  7. customleaving a gum
  8. temperatureThe solution is heated
  9. customresults
  10. temperatureThe mixture is cooled
  11. filtrationfiltered
  12. customto yield 3.6 g

출처 및 근거

ORD 기록
ord-1bafe3e871e941419282988b01d2d9ba
출처 데이터셋
uspto-grants-1982_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04348527

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