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Ammonium Chloride → 1-[5-(2-Bromophenyl)-1,5-dioxopentyl]pyrrolidine

HRID 1722343
ノート
印刷プレビュー

反応式

HRID 1722343 の反応式
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13](=[O:21])[CH2:14][CH2:15][CH2:16][C:17](OC)=[O:18].[NH4+].[Cl-]>>[Br:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[C:13](=[O:21])[CH2:14][CH2:15][CH2:16][C:17]([N:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1)=[O:18]
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 3

HCID 25517Ammonium Chloride2 回HCID 31268Pyrrolidine2 回HCID 14582851Methyl 2-bromo-delta-oxobenzenepentanoate

生成物 1

HCID 150876271-[5-(2-Bromophenyl)-1,5-dioxopentyl]pyrrolidine

実験手順

To 1ml of pyrrolidine is added with stirring 0.100g (0.35 mmol) of the product of Example 3, and 5mg of NH4Cl. The combined reagents were stirred in a sealed tube for 16 hours at room temperature. After this time, an additional 1ml of pyrrolidine and 5mg of NH4Cl was added and the reaction mixture was stirred an additional 16 hours. The solvent was removed under reduced pressure and the residue was flash chromatographed. Elution with diethyl ether produced 0.13g of the titled product, which was used without further purification.

後処理

  1. stirringthe reaction mixture was stirred an additional 16 hours
  2. customThe solvent was removed under reduced pressure
  3. customchromatographed
  4. washElution with diethyl ether

出典と根拠

ORDレコード
ord-c07a163162294d7b9c2f9c20125ba723
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04855324

反応ノート

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