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

HRID 1073645
ノート
印刷プレビュー

反応式

HRID 1073645 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 1 ml of pyrrolidine is added with stirring 0.100 g (0.35 mmol) of the product of Example 3, and 5 mg of NH4Cl. The combined reagents were stirred in a sealed tube for 16 hours at room temperature. After this time, an additional 1 ml of pyrrolidine and 5 mg 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 0.13 g 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-4bacad5adc7c4d36b4604b6f4117a866
出典データセット
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04970234

反応ノート

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