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3-(Dimethylamino)-2-propenal → HCID 178467801、化合物

HRID 406520
ノート
印刷プレビュー

反応式

HRID 406520 の反応式
[F:1][B-:2]([F:5])([F:4])[F:3].[NH+]1C=CC=CC=1.[CH3:12][N:13]([CH3:19])/[CH:14]=[CH:15]/[C:16](=[O:18])[CH3:17].[CH3:20][N:21]([CH3:26])[CH:22]=[CH:23][CH:24]=O>C(OC(=O)C)(=O)C.C(O)(=O)C>[F:1][B-:2]([F:5])([F:4])[F:3].[CH3:12][N:13]([CH3:19])[CH:14]=[C:15]([C:16](=[O:18])[CH3:17])[CH:24]=[CH:23][CH:22]=[N+:21]([CH3:26])[CH3:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 791253-(Dimethylamino)-2-propenalHCID 5369152trans-4-(Dimethylamino)-3-buten-2-oneHCID 11019233Borate(1-), tetrafluoro-, hydrogen, compd. with pyridine (1:1:1)

生成物 1

HCID 178467801HCID 178467801、化合物収率 96%

試薬・触媒・溶媒 1

HCID 21895370AcOH AcOAc溶媒

反応条件

温度
0 °C

実験手順

Pyridinium tetrafluoroborate (2.21 g, 13.3 mmol) was added to a solution of (3E)-4-(dimethylamino)-3-buten-2-one (1.54 ml, 13.3 mmol) in 13.5 ml acetic anhydride/acetic acid (2:1). The resulting suspension was cooled to 0° C. and 3-dimethylaminoacroleine (1.33 ml, 13.3 mmol) was added over a period of 1 h under vigorous stirring and cooling with an ice bath receiving a red-brown precipitate. The cool reaction mixture was filtered and the remaining solid was washed with diethylether several times and dried under reduced pressure. The pentamethinium salt was obtained as orange crude product (2.69 g, 96%) and was used without any further purification.

後処理

  1. temperaturecooling with an ice bath
  2. customThe cool reaction mixture
  3. filtrationwas filtered
  4. washthe remaining solid was washed with diethylether several times
  5. customdried under reduced pressure

出典と根拠

ORDレコード
ord-cd552ca6e27549e988c610e8cce96ebb
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08754111B2

反応ノート

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