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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tributylamine → HCID 178509618, 화합물

HRID 857926
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HRID 857926 반응식
[NH2:1][C:2]1[N:6]=[CH:5][NH:4][N:3]=1.[C:7]([C:9]1[CH:14]=[CH:13][C:12]([CH:15]([C:21](OCC)=[O:22])[C:16](OCC)=[O:17])=[CH:11][CH:10]=1)#[N:8].C(N(CCCC)CCCC)CCC.[OH-].[Na+]>O>[OH:17][C:16]1[C:15]([C:12]2[CH:13]=[CH:14][C:9]([C:7]#[N:8])=[CH:10][CH:11]=2)=[C:21]([OH:22])[N:3]2[N:4]=[CH:5][N:6]=[C:2]2[N:1]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7622TributylamineHCID 14798Sodium HydroxideHCID 11737076Diethyl (4-cyanophenyl)propanedioateHCID 178418311HCID 178418311, 화합물

생성물 1

HCID 178509618HCID 178509618, 화합물수율 66.4%

시약·촉매·용매 1

HCID 962Water용매

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온도
180 °C

실험 절차

A mixture of 14 g of 3-amino-1,2,4-triazole, 0.17 mol of the ester from example 1 and 50 ml of tributylamine (50 ml) was stirred at 180° C. for approximately 6 hours. A solution of 21 g of NaOH in 200 ml of water was added at approximately 700 and the mixture was stirred for a further 30 min. The organic phase was separated and the aqueous phase was extracted with diethyl ether. The product precipitated from the aqueous phase after acidification with concentrated hydrochloric acid. 28 g of the title compound were obtained by filtration.

후처리

  1. stirringthe mixture was stirred for a further 30 min
  2. customThe organic phase was separated
  3. extractionthe aqueous phase was extracted with diethyl ether
  4. customThe product precipitated from the aqueous phase after acidification with concentrated hydrochloric acid

출처 및 근거

ORD 기록
ord-35e276461e314910b85204b5b4f94f03
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07148227B2

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