참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Tributyl borate | HCID 12712 | — |
| 반응물 | 2-Chloro-2-butenal | HCID 94558 | — |
| 반응물 | Benzenesulfonyl cyanide | HCID 10313279 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | 2-Benzenesulfonyl-5-chloropyridine | HCID 10198940 | 69.9% |
반응 단계
First, 11.2 g (107 mmol) of 2-chloro-2-butenal and 8.35 g (50.0 mmol) of benzenesulfonyl cyanide were introduced to the same reaction vessel as in Example 1. Toluene (15 ml) as the solvent and butanol (1.5 ml) were added, and 1.30 g (5.65 mmol) of tributyl borate was added. Then the mixture was heated under reflux for 7 hours while agitating at an internal temperature of 121° C. in a nitrogen atmosphere, separating and removing water that was produced. After this solution was cooled to room temperature, the low-boiling components, such as solvent, etc., were removed under reduced pressure and the resulting concentrate was cooled in an ice bath to precipitate crystals. The crystals were filtered with a glass filter and washed with 10 ml toluene that had been cooled to 5° C. or lower. Then the crystals were dried for 2 hours in vacuo to give 8.87 g of 2-benzenesulfonyl-5-chloropyridine with the following properties as colorless crystals (purity of 98%, yield of 69% based on benzenesulfonyl cyanide).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06197962B1 |
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| 출처 데이터셋 | uspto-grants-2001_03 |
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| ORD ID | ord-68eb82cd563648b09746a17e5b4e9ec6 |
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| 출처 메모 | uspto-grants-2001_03 |
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