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4,4-Diethoxybutylamine → HCID 57950350、化合物

HRID 1020702
ノート
印刷プレビュー

反応式

HRID 1020702 の反応式
C(O[CH:4](OCC)[CH2:5][CH2:6][CH2:7][NH2:8])C.Cl.[Br:13][C:14]1[CH:15]=[C:16]([NH:21]N)[CH:17]=[CH:18][C:19]=1[F:20]>CO>[Br:13][C:14]1[CH:15]=[C:16]2[C:17]([C:5]([CH2:6][CH2:7][NH2:8])=[CH:4][NH:21]2)=[CH:18][C:19]=1[F: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

4

反応物 2

HCID 806724,4-DiethoxybutylamineHCID 67250486(3-Bromo-4-fluorophenyl)hydrazine hydrochloride

生成物 1

HCID 57950350HCID 57950350、化合物収率 116.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
180 °C

実験手順

4,4-Diethoxybutan-1-amine (4.72 g, 29.3 mmol) was added to (3-bromo-4-fluorophenyl)hydrazine hydrochloride (6.4 g, 27 mmol). The resulting mixture in an open round bottom flask was placed into a preheated oil bath at 180° C. The mixture was stirred at 180° C. for 2.5 h and then cooled to 120° C. Methanol (300 mL) was added, and the mixture was stirred at ambient temperature for 18 h. The resulting suspension was filtered through a silica gel plug, and the silica gel was then washed with methanol (5×300 mL). The combined methanol fractions were concentrated under vacuum to provide the crude title compound (8.1 g) as a yellow solid, which was used in the next step without further purification: ESI MS m/z 257 [M+H]+.

後処理

  1. customThe resulting mixture in an open round bottom flask was placed into a preheated oil bath at 180° C
  2. temperaturecooled to 120° C
  3. stirringthe mixture was stirred at ambient temperature for 18 h
  4. filtrationThe resulting suspension was filtered through a silica gel plug
  5. washthe silica gel was then washed with methanol (5×300 mL)
  6. concentrationThe combined methanol fractions were concentrated under vacuum

出典と根拠

ORDレコード
ord-43f1710483614ea08ece6c672493485f
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08716308B2

反応ノート

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