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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Malonate → HCID 20335826, 화합물

HRID 1706415
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HRID 1706415 반응식
[C:1](OCC)(=O)CC(OCC)=O.[H-].[Na+].[C:14]([C:22]1[C:27]([N+:28]([O-:30])=[O:29])=[CH:26][CH:25]=[C:24](Cl)[N:23]=1)(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>O1CCOCC1>[C:14]([C:22]1[C:27]([N+:28]([O-:30])=[O:29])=[CH:26][CH:25]=[C:24]([CH3:1])[N:23]=1)(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7761Diethyl MalonateHCID 24758Sodium hydrideHCID 20520021HCID 20520021, 화합물

생성물 1

HCID 20335826HCID 20335826, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

They were added to a solution of 16.8 grams of diethyl malonate in 75 ml. of dioxane with stirring and under a nitrogen atmosphere 3.3 grams of sodium hydride (80%) and then stirring continued for 15 minutes more. Then there were added in portions 26.3 grams of 2-benzoyl-3-nitro-6-chloropyridine and then stirring was continued at 70° C. for two hours more. The precipitated deeply colored sodium salt of the dicarbethoxymethyl compound was filtered off with suction. Five grams of this compound were boiled under reflux in a mixture of 25 ml. of concentrated hydrochloric acid and 25 ml. of methanol for 90 minutes, the solution filtered hot and the filtrate treated with water to the point of turbidity. The desired product crystallized out.

후처리

  1. stirringstirring
  2. waitwas continued at 70° C. for two hours
  3. customThe precipitated deeply colored sodium salt of the dicarbethoxymethyl compound
  4. filtrationwas filtered off with suction
  5. temperatureunder reflux in a mixture of 25 ml
  6. waitof methanol for 90 minutes
  7. filtrationthe solution filtered hot
  8. additionthe filtrate treated with water to the point of turbidity
  9. customThe desired product crystallized out

출처 및 근거

ORD 기록
ord-55af05183c294022a3f4d3f036043ba1
출처 데이터셋
uspto-grants-1980_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04207322

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