戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 895466作成日:2026年10月26日

Acetic Acid → Tert-butyl 4-[(3-chlorophenyl)methyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/895466

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3-ChlorobenzaldehydeHCID 11477—
反応物Sodium HydroxideHCID 14798—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,1-DichloroethaneHCID 6365—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 4-[(3-chlorophenyl)methyl]piperazine-1-carboxylateHCID 431694087.4%

反応手順

To a solution of piperazine-1-carboxylic acid tert-butyl ester (4.00 g, 21.5 mmol) in dry dichloroethane (70 mL) are added 3-chlorobenzaldehyde (2.49 mL, 3.08 g, 21.9 mmol), HOAc (2.58 mL, 2.71 g, 45.1 mmol) and NaBH(OAc)3 (5.46 g, 25.8 mmol) at ambient temperature. After stirring at ambient temperature for 3d, 2N NaOH (40 mL) is added, the layers are separated, and the aqueous layer is extracted with CH2Cl2 (4×50 mL). The combined organic extracts are washed with water (3×50 mL) and brine (80 mL) and dried over MgSO4. The crude material is purified by chromatography on silica gel, eluting with hexane:EtOAc mixtures, yielding 5.83 g (18.8 mmol, 87%) of the title compound as yellow oil. MS (ES): m/z 311.0/313.0 (50/18) [MH+]. tR (method A)=5.0 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06916804B2
出典データセットuspto-grants-2005_07
ORD IDord-1de5866408e84ce6b7262895363e3a82
出典メモuspto-grants-2005_07