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HRID 646659作成日:2026年10月26日

1,2-Dichlorobenzene → Sulphenone

https://huagongshe.com/reaction/646659

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichlorobenzeneHCID 7239—
反応物1-Benzenesulfonyl-4-phenoxy-benzeneHCID 628195—
溶媒1,2,4-TrichlorobenzeneHCID 13—
溶媒1,2,3-TrichlorobenzeneHCID 6895—
溶媒Benzene, 1,2-dichloro-4-methyl-HCID 7256—
生成物SulphenoneHCID 6621—

反応手順

FIGS. 1 and 2 illustrate the behavior of the new phase transfer catalysts in the formation of 1,1′-(1-methylethylidene)bis[4-[4-(phenylsulfonyl)phenoxy]benzene (CAS No. 90139-53-0). When the P2-EthylMethyl mesylate was used as a PTC at 1.0 mole % in the model reaction in refluxing o-DCB at 180° C. (See 4 (FIG. 1)), the reaction exhibited pseudo-first order kinetics. This indicates that no catalyst decomposition nor diminution in rate was occurring during the reaction. In order to further test the stability of the phosphazenium salt, similar reactions were carried out at higher temperatures, in 3,4-dichlorotoluene (bp=200° C.) (See 6 (FIG. 1)) and in 1,2,4-trichlorobenzene (bp=214° C.) (See 2 (FIG. 1)). As shown in FIG. 1, even at 200° C., essentially linear reaction kinetics were observed, indicating no decomposition of the P2-EthylMethyl mesylate phase transfer catalyst. In trichlorobenzene, only a small amount of decomposition was observed, after 60 minutes (See 2 (FIG. 1)). In this instance only 0.5 mole % catalyst was used, since after initial range-finding experiments it was determined that reaction using 1.0 mole % would be too fast to follow accurately at 214° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07705190B2
出典データセットuspto-grants-2010_04
ORD IDord-d489113f7fe0433aacb63f30a216fb3e
出典メモuspto-grants-2010_04