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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetamide → 1,3,5-Triazine-2-carbonitrile, 4,6-dimethoxy-

HRID 2413076
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HRID 2413076 반응식
[C-]#N.[K+].[C:4]([NH2:7])(=O)C.[Cl-].C[N+](C)(C)[C:11]1[N:16]=[C:15]([O:17][CH3:18])[N:14]=[C:13]([O:19][CH3:20])[N:12]=1>O>[C:4]([C:11]1[N:12]=[C:13]([O:19][CH3:20])[N:14]=[C:15]([O:17][CH3:18])[N:16]=1)#[N:7]
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참가 물질

5

반응물 3

HCID 178AcetamideHCID 9032Potassium CyanideHCID 131413314,6-Dimethoxy-N,N,N-trimethyl-1,3,5-triazin-2-aminium chloride

생성물 1

HCID 23202681,3,5-Triazine-2-carbonitrile, 4,6-dimethoxy-수율 38.3%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 26 g of potassium cyanide and 60 g of oven-dried acetamide was heated to 85°-90° C. To this melt was added 24 g of the product from Example 2 in portions over a period of 15-20 minutes. The resulting brown reaction solution was heated to 90°-100° C. for an additional one hour. When the solution had cooled to room temperature, water was added and the aqueous layer was extracted with ether and methylene chloride. The combined organic extracts were backwashed with several small portions of water, brine, and were then dried over magnesium sulfate and concentrated in vacuo to afford 6.5 g of 2-cyano-4,6-dimethoxy-1,3,5-triazine as a light yellow solid.

후처리

  1. temperaturewas heated to 85°-90° C
  2. temperatureThe resulting brown reaction solution was heated to 90°-100° C. for an additional one hour
  3. extractionthe aqueous layer was extracted with ether and methylene chloride
  4. dry with materialwere then dried over magnesium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-232248879c4f4b3d86c8de105672fe7c
출처 데이터셋
uspto-grants-1985_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04496392

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