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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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((Dimethylamino)methylene)dimethylammonium methyl sulphate → 1066-47-3

HRID 1477407
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인쇄 미리보기

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HRID 1477407 반응식
COS([O-])(=O)=O.[CH3:7][N:8]([CH3:13])[CH:9]=[N+:10]([CH3:12])[CH3:11].[F:14][P-:15]([F:20])([F:19])([F:18])([F:17])[F:16].[NH4+]>O>[F:14][P-:15]([F:20])([F:19])([F:18])([F:17])[F:16].[CH3:11][N:10]([CH3:12])[CH:9]=[N+:8]([CH3:13])[CH3:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3014065((Dimethylamino)methylene)dimethylammonium methyl sulphateHCID 9793912Ammonium hexafluorophosphate

생성물 1

HCID 866270241066-47-3

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
0 °C

실험 절차

N,N,N′,N′-tetramethylformamidinium methylsulfate (3 g) is added to water (25 ml) and the resulting mixture is cooled to 0° C. This mixture is then added to a cooled solution of ammonium hexafluorophosphate (4.6 g) in water (25 ml). The so formed precipitate is then collected by filtration. The precipitate is washed with cold water (2×10 ml) and then with diethyl ether (10 ml). Drying in vacuo gives N,N,N′,N′-tetramethylformamidinium hexafluorophosphate (18, R6=Me, R7=Me) as a white solid. 1H NMR (DMSO-d6), 7.90 (1H), 3.26 (6H), 3.14 (6H).

후처리

  1. customThe so formed precipitate
  2. filtrationis then collected by filtration
  3. washThe precipitate is washed with cold water (2×10 ml)
  4. customDrying in vacuo

출처 및 근거

ORD 기록
ord-0ed59cae49c14dd0bf74abf94aaea844
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09403766B2

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