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HRID 223317作成日:2026年10月26日

1-Phenyl-1,2-ethanediol → 1,2-Hexanediol

https://huagongshe.com/reaction/223317

反応式

関与物質

役割名称HCID仕込み量
反応物1-Phenyl-1,2-ethanediolHCID 7149—
反応物3-Chloro-1,2-propanediolHCID 7290—
反応物HexachloroacetoneHCID 8303—
生成物1,2-HexanediolHCID 94335—
生成物4-Phenyl-1,3-dioxolan-2-oneHCID 234226—

反応手順

Similarly, 1,2-butanediol and 2,3-butanediol were heated with equivalent quantities of hexachloroacetone in the presence of K2CO3 or other such basic catalyst as previously defined to produce comparable yields of 1,2-butylene carbonate and 2,3-butylene carbonate, respectively. Also, 3-chloro-1,2-propanediol was reacted in this way with hexachloroacetone to make 4-(chloromethyl)-1,3-dioxol-2-one (chloromethylethylene carbonate). In the same way, styrene glycol (1-phenyl-1,2-ethanediol) is reacted with hexachloroacetone in the presence of a basic catalyst to produce 1-phenylethylene carbonate (4-phenyl-1,3-dioxol-2-one), 1,2-hexanediol is reacted with hexachloroacetone to produce 1,2-hexylene carbonate (4-butyl-1,3-dioxol-2-one), and 1-cyclohexyl-1,2-ethanediol is reacted with hexachloroacetone to make 4-cyclohexyl-1,3-dioxol-2-one (cyclohexylethylene carbonate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04353831
出典データセットuspto-grants-1982_10
ORD IDord-f0c9e1a7c5e847a18bf2a1a6a28f2ab7
出典メモuspto-grants-1982_10