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Dimethylformamide dimethyl acetal → N'-(2-Cyano-3,6-difluorophenyl)-N,N-dimethylformamidine

HRID 1467398
ノート
印刷プレビュー

反応式

HRID 1467398 の反応式
[NH2:1][C:2]1[C:9]([F:10])=[CH:8][CH:7]=[C:6]([F:11])[C:3]=1[C:4]#[N:5].CO[CH:14](OC)[N:15]([CH3:17])[CH3:16]>C1(C)C=CC=CC=1>[C:4]([C:3]1[C:6]([F:11])=[CH:7][CH:8]=[C:9]([F:10])[C:2]=1[N:1]=[CH:14][N:15]([CH3:17])[CH3:16])#[N:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 78373Dimethylformamide dimethyl acetalHCID 450905912-Amino-3,6-difluorobenzonitrile

生成物 1

HCID 59223042N'-(2-Cyano-3,6-difluorophenyl)-N,N-dimethylformamidine収率 797.9%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A solution of 2-amino-3,6-difluorobenzonitrile (1.92 g, 12.5 mmol) and N,N-dimethylformamide dimethyl acetal (2.2 mL, 1.3 mmol) in 15 mL of toluene was heated to reflux for 1 h. The reaction was complete based on GC-MS. The solvent was removed in vacuo and the oily residue was suspended in hexane and a small amount of ether. The mixture was then cooled in a freezer for 20 min. The resulting solid was suction filtered, washed with hexane and dried to give 2.17 g (83% yield) of the product as a tan solid, M.P. 56-60°; GC/MS: m/z 209. 1H NMR (CDCl3): δ 7.86 (s, 1H), 7.16 (m, 1H), 6.63 (m, 1H), 3.12 (s, 3H), 3.10 (s, 3H).

後処理

  1. temperatureto reflux for 1 h
  2. customThe solvent was removed in vacuo
  3. temperatureThe mixture was then cooled in a freezer for 20 min
  4. filtrationfiltered
  5. washwashed with hexane
  6. customdried

出典と根拠

ORDレコード
ord-230581bf8a63471ca9c3efcd8aacc418
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09000162B2

反応ノート

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