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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 646659생성일: 2026년 10월 26일

1,2-Dichlorobenzene → Sulphenone

https://huagongshe.com/reaction/646659

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichlorobenzeneHCID 7239—
반응물1-Benzenesulfonyl-4-phenoxy-benzeneHCID 628195—
용매1,2,4-TrichlorobenzeneHCID 13—
용매1,2,3-TrichlorobenzeneHCID 6895—
용매Benzene, 1,2-dichloro-4-methyl-HCID 7256—
생성물SulphenoneHCID 6621—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705190B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-d489113f7fe0433aacb63f30a216fb3e
출처 메모uspto-grants-2010_04