Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1258379생성일: 2026년 10월 27일
2-Chloro-1,4-naphthoquinone → N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide
https://huagongshe.com/reaction/1258379
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Chloro-1,4-naphthoquinone | HCID 13891 | — |
| 반응물 | 2-Thiophenesulfonamide | HCID 72881 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide | HCID 697416 | 55.9% |
반응 단계
385.2 mg 2-chloro-1,4-naphthoquinone (11) was mixed with 326.4 mg thiophene-2-sulfonamide in 15 ml dichloromethylene, to which at 0° C. was added 2 ml TiCl4 dichloromethylene solution followed by 613.3 μl. The mixture was heated at 60° C. with M.W. for 15 min and the black mixture was poured into 100 ml ethyl acetate. The insoluble was removed by filtrate through a pad of celite. The filtrate was concentrated and the residue was suspended in dichloromethylene. The brown insoluble stuff was removed by filtration and the filtrate was again concentrated to dryness. The residue was suspended in ethyl acteate/hexane (1:1) and the yellow solid was filtered. The solid was washed with ethyl acteate/hexane (1:1) and dried over vacuum affording title compound 377.7 mg (55.9%) as a yellow solid. When TiCl4.2THF and THF were used instead, the reaction afforded the title compound 522 mg (77.3%) as a yellow solid, m.p.: 167-169° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08466157B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-2bcc240fbb1f45b79d13853668afa919 |
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| 출처 메모 | uspto-grants-2013_06 |
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