戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1531381作成日:2026年10月26日

Toluene → 2-Benzenesulfonyl-5-chloropyridine

https://huagongshe.com/reaction/1531381

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Tributyl borateHCID 12712—
反応物2-Chloro-2-butenalHCID 94558—
反応物Benzenesulfonyl cyanideHCID 10313279—
溶媒1-ButanolHCID 263—
生成物2-Benzenesulfonyl-5-chloropyridineHCID 1019894069.9%

反応条件

温度121 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06197962B1
出典データセットuspto-grants-2001_03
ORD IDord-68eb82cd563648b09746a17e5b4e9ec6
出典メモuspto-grants-2001_03