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Trichlorofluoromethane → Agn-PC-0nfb2Y

HRID 1285287
ノート
印刷プレビュー

反応式

HRID 1285287 の反応式
[Cl:1][C:2]([Cl:5])([Cl:4])F.[Cl:6][C:7]([F:11])=[C:8]([F:10])[Cl:9].ClC(F)=C(F)[F:15]>C(Cl)(Cl)(Cl)Cl>[F:10][C:8]([Cl:9])([F:15])[C:7]([Cl:6])([F:11])[C:2]([Cl:5])([Cl:4])[Cl:1]
参加物実験手順出典と根拠反応ノート

参加物

5

反応物 3

HCID 6389TrichlorofluoromethaneHCID 6594ChlorotrifluoroethyleneHCID 11736Dichlorodifluoroethene

生成物 1

HCID 11065502Agn-PC-0nfb2Y

試薬・触媒・溶媒 1

HCID 5943Carbon Tetrachloride溶媒

実験手順

a process wherein trichlorofluoromethane is added to 1,2-dichlorodifluoroethylene or carbon tetrachloride is added to chlorotrifluoroethylene to obtain 1,1,2-trifluoropentachloropropane, which is then oxidized and esterified to form a 2,3-dichlorotrifluoropropionic acid ester, followed by dechlorination of the ester; (2) a process wherein bromine is added to chlorotrifluoroethylene to obtain 1,2-dibromo-1-chlorotrifluoroethylene, which is then subjected to an addition reaction with propylene, followed by dehydrobromination to obtain 5-bromo-4-chloro-4,5,5-trifluoropentene-2 (CF2BrCFClCH=CHCH3), which is then oxidized and esterified to form a 3-bromo-2-chlorotrifluoropropionic acid ester, which is in turn dehalogenated; and (3) a process wherein chlorotrifluoroethylene is subjected to an addition reaction with hydrogen bromide, followed by dehalogenation to obtain trifluoroethylene, which is then subjected to an addition reaction with ICl, followed by dehydrochlorination to obtain trifluoroiodoethylene, which is then reacted with metallic magnesium in ether to form an organomagnesium intermediate, which is in turn reacted with carbon dioxide, followed by hydrolysis to obtain perfluoroacrylic acid, which is then esterified.

出典と根拠

ORDレコード
ord-eef21d5b2b2847aa8d4951b0fe7b9bcf
出典データセット
uspto-grants-1986_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04567003

反応ノート

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