Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4816생성일: 2026년 10월 23일
Lawesson's reagent → 7-Chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)thione
https://huagongshe.com/ko/reaction/4816
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Lawesson's reagent | HCID 87949 | — |
| 반응물 | 7-Chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-one | HCID 13726445 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 7-Chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)thione | HCID 13726448 | — |
반응 단계
7-Chloro-2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido [3,2-f][1,4]oxazepin-5(4H)-one, 6.0 g (0.022 mole) was suspended in 200 ml of toluene. To this suspension was added 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-dilsulfide. The mixture was heated to reflux with vigorous stirring for 2 hours. Because the reaction was not complete, an additional amount (3.0 g) of 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide was added and the mixture stirred at reflux for 2 hr and left standing for 56 hr at room temperature. The toluene layer was decanted and washed with 50 ml of dilute aqueous sodium hydroxide and 50 ml of dilute hydrochloric acid. Toluene was removed by rotary evaporation (~80° C., water aspirator). The crude oil was recrystallized from isopropyl alcohol giving 3.5 g (54%) of pale yellow crystals, m.p. 125°-127° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04727152 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-d509aa5423c6487cbbe6785e60b235b3 |
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| 출처 메모 | uspto-grants-1988_02 |
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