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HRID 7640作成日:2026年10月24日

3-Chloro-2-chloromethyl-1-propene → Benzyl tert-butyl 4-methylidenepyrazolidine-1,2-dicarboxylate

https://huagongshe.com/ja/reaction/7640

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-2-chloromethyl-1-propeneHCID 15859—
反応物Sodium hydrideHCID 24758—
反応物Benzyl tert-butyl hydrazine-1,2-dicarboxylateHCID 11288582—
溶媒DimethylformamideHCID 6228—
生成物Benzyl tert-butyl 4-methylidenepyrazolidine-1,2-dicarboxylateHCID 12970152—

反応手順

To a suspension of NaH (3.81 g, 95.4 mmol) in DMF (80 mL) is add dropwise a solution of N-Cbz-N′-Boc-hydrazine (12.1 g, 45.4 mmol) in DMF (20 mL). The reaction mixture is stirred about 20 minutes and 3-chloro-2-chloromethyl-propene (5.8 mL, 50 mmol) is added dropwise and the reaction is allowed to stir at room temperature until the reaction is complete by TLC, approximately 12 hours. The reaction solution is partitioned between ethyl acetate and water, the water layer being extracted several times more with solvent. The combined organic layers are dried, filtered, and concentrated to afford the desired product as a clear oil which is used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087615B2
出典データセットuspto-grants-2006_08
ORD IDord-16ce0de6403640198e3f969730ca292f
出典メモuspto-grants-2006_08