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HRID 393829作成日:2026年10月25日

Benzenesulfonyl chloride → 4-(1,1-Dimethylethyl)-benzoic acid, 2-(phenylsulfonyl)hydrazide

https://huagongshe.com/reaction/393829

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chlorideHCID 7369—
反応物DiisopropylethylamineHCID 81531—
反応物Benzoic acid, 4-(1,1-dimethylethyl)-, hydrazideHCID 123513—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TetrahydrofuranHCID 8028—
生成物4-(1,1-Dimethylethyl)-benzoic acid, 2-(phenylsulfonyl)hydrazideHCID 923503—

反応条件

温度0 °C

反応手順

4-tert-Butyl-benzoic acid hydrazide (0.5 g, 2.60 mmol) was dissolved in THF (29 mL). N,N-diisopropylethylamine (1.81 mL, 10.4 mmol) was added, and the reaction was cooled to 0° C. Phenylsulfonyl chloride (0.36 mL, 2.86 mmol) was added followed by DMAP (5 mg, 0.04 mmol). The reaction was allowed to warm to room temperature, and the reactants all dissolved. The solution went from a yellow color to a deep red over the course of 4 hours. The reaction was then concentrated down and purified by flash chromatography eluting with 3:1 hexanes/EtOAc. The desired product was isolated (0.32 g, 37.1%). MS: 333.1 (M+1 for C17H20N2O3S); mp 197-199° C.; TLC: SiO2 Rf=0.56 (1:1 hexane/EtOAc). Analysis C17H20N2O3S: (calc) C, 61.42; H, 6.06; N, 8.43. (found) C, 61.38; H, 6.09; N, 8.27. IR (KBr, cm−1) 3213, 2965, 1648, 1403, 1349, 1179. 1H NMR (400 MHz, CDCl3) δ 1.29 (s, 9H), 7.39-7.55 (m, 8H), 7.92-7.93 (m, 2H), 8.06 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809119B2
出典データセットuspto-grants-2004_10
ORD IDord-f622c312826c4955b8b81db1e9b3f7e5
出典メモuspto-grants-2004_10