Benzene → Butyrophenone

HRID 256211

反応式

HRID 256211 の反応式
C(C1C=CC=CC=1C=C)=C.[CH:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[C:17](Cl)(=[O:21])[CH2:18][CH2:19][CH3:20]>[Cl-].[Al+3].[Cl-].[Cl-]>[CH2:18]([C:17]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:21])[CH2:19][CH3:20]

参加物

5

反応物 3

HCID 241BenzeneHCID 8855Butyryl chlorideHCID 666661,2-Diethenylbenzene

生成物 1

HCID 10315Butyrophenone

試薬・触媒・溶媒 1

HCID 6451240Aluminum(III) Chloride触媒

実験手順

About 50 grams of resin beads of polystyrene that has been copolymerized with about 1% divinylbenzene are stirred at room temperature for about 2 hours in butyryl chloride with aluminum chloride as a catalyst, namely Friedel-Crafts conditions. Reaction occurs with the benzene moieties on the resin to form butyrophenone or propylphenylketone. These resulting ketone moieties are then subjected to the Leukardt-Wallach reduction amination reaction using N-propyl formamide to produce N-propyl α-aminobenzyl moieties. The step-by-step synthesis of the nonapeptide as set forth in Example I is repeated. Cleavage, deprotection and purification are carried out under the same conditions and are found to produce the nonapeptide amide having the following formula:

後処理

  1. customReaction

出典と根拠

ORDレコード
ord-391515ef7ed54614934d87ce74b4052c
出典データセット
uspto-grants-1987_10
特許番号
US04701499

関連ノート

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