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HRID 1361484作成日:2026年10月26日

1,4-Dioxane → 1-(4-Chlorobenzoyl)piperazine

https://huagongshe.com/reaction/1361484

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物tert-Butyl 4-(4-chlorobenzoyl)piperazine-1-carboxylateHCID 49814251—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Chlorobenzoyl)piperazineHCID 410148499%

反応手順

4-(4-Chloro-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester (26 g) was dissolved in CH2Cl2 (350 mL). 4M HCL/Dioxane (150 mL) was added. The mixture was stirred at RT for 4 h. White precipitate was formed. The mixture was concentrated. The white solid was washed with Et2O. After the white solid was treated with 1N NaOH (200 mL) and extracted with Ethyl acetate (3×100 mL), the combined organic phase was dried over Na2SO4 and concentrated to give 17.79 g of desired product (99% yield). 1H-NMR (for HCl salt) (300 MHz, MeOD): δ 2.80-2.90 (m, 4 H), 3.20-3.80 (m, 4 H), 7.29-7.36 (m, 4 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07880002B2
出典データセットuspto-grants-2011_02
ORD IDord-7f4e8e32b7c6442dbc5d21a19205abd7
出典メモuspto-grants-2011_02