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Propanal → [1-(4-Bromophenyl)-cyclopropyl]dipropylamine

HRID 278765
ノート
印刷プレビュー

反応式

HRID 278765 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([NH2:11])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[CH2:12]1[CH2:16]OC[CH2:13]1.[CH:17](=O)[CH2:18][CH3:19].[BH3-]C#N.[Na+]>CC#N.CC(O)=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2([N:11]([CH2:13][CH2:12][CH3:16])[CH2:17][CH2:18][CH3:19])[CH2:9][CH2:10]2)=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 527PropanalHCID 8028TetrahydrofuranHCID 5003444Sodium cyanoborohydrideHCID 187101951-(4-Bromophenyl)cyclopropanamine2 回

生成物 1

HCID 22568796[1-(4-Bromophenyl)-cyclopropyl]dipropylamine

試薬・触媒・溶媒 1

HCID 22391770Acetonitrile aceticacid溶媒

実験手順

To a solution of 1-(4-bromophenyl)-cyclopropylamine (Intermediate 116) in CH3CN/HOAc (5 mL, 9:1, v/v) and THF 3 mL at 0° C. was added propionaldehyde (277.0 mg, 4.95 mmols) and NaCNBH3(153.0 mg, 2.47 mmols). The reaction was warmed to room temperature and after 5 hours quenched with H2O. The pH of the solution was adjusted to 8-9 using aqueous NaOH and extracted with EtOAc. The combined extracts were washed with H2O and saturated aqueous NaCl, dried (MgSO4) and concentrated under reduced pressure. The title compound, 190.0 mg (56%), was isolated by column chromatography (2-5% EtOAc-hexanes).

後処理

  1. customquenched with H2O
  2. extractionextracted with EtOAc
  3. washThe combined extracts were washed with H2O and saturated aqueous NaCl
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-193144e904074215b441248e10d085b5
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06359135B1

反応ノート

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