戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 964084作成日:2026年10月26日

3,5-Di-tert-butyl-4-hydroxybenzoic acid → 4-[3-(3,5-Di-t-butyl-4-hydroxybenzoylamino)propylthio]pyridine

https://huagongshe.com/reaction/964084

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
反応物N-HydroxysuccinimideHCID 80170—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物4-(3-Aminopropylthio)pyridineHCID 15227695—
溶媒DichloromethaneHCID 6344—
生成物4-[3-(3,5-Di-t-butyl-4-hydroxybenzoylamino)propylthio]pyridineHCID 1907915927.3%

反応手順

To a solution of 1.49 g (5.94 mmol) of 3,5-di-t-butyl-4-hydroxybenzoic acid and 889 mg (7.73 mmol) of N-hydroxysuccinimide in 60 ml of methylene chloride was added 1.38 g (7.13 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. Further 1.00 g (5.94 mmol) of 4-(3-aminopropylthio)pyridine was added and the mixture was stirred at room temperature for 8 hours. The reaction mixture was washed with water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 650 mg of the desired compound (27.3%, colorless powder), mp: 203.0°-204.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05767121
出典データセットuspto-grants-1998_06
ORD IDord-7d6019a4f0d04fd2b40f36bcbd580c56
出典メモuspto-grants-1998_06