戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 399772作成日:2026年10月26日

3-Bromophenylhydrazine hydrochloride → 4-(3-Bromophenyhydrazono)-1-butanol

https://huagongshe.com/reaction/399772

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromophenylhydrazine hydrochlorideHCID 33757—
反応物2,3-DihydrofuranHCID 70934—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3-Bromophenyhydrazono)-1-butanolHCID 6761318199.6%

反応手順

Under anhydrous conditions a solution of 3-bromophenylhydrazine hydrochloride (22.5 g, 100 mmol) and 2,3-dihydrofuran (7.55 ml, 100 mmol) in 200 ml of dry THF was stirred at ambient temperature for 3 h. The reaction mixture was partitioned between EtOAc and H2O. The organic phase was washed with H2O and brine. After drying (Na2 SO4), the solvent was evaporated to give 25.6 g of the product as a brown oil. The product was of suitable purity for use in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05824699
出典データセットuspto-grants-1998_10
ORD IDord-71f44accceb34da08c5f8b2e174c5c94
出典メモuspto-grants-1998_10