戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 14283作成日:2026年10月25日

Triethylborane → Cyclopropyl m-ethylbenzylamine

https://huagongshe.com/reaction/14283

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylboraneHCID 7357—
反応物TetrahydrofuranHCID 8028—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Boc-bromobenzyl amineHCID 54140302—
生成物Cyclopropyl m-ethylbenzylamineHCID 21086019—

反応手順

The Boc-bromobenzyl amine 10 (26.8 g, 94.03 mmol), and PddfPdC12 (816 mg, 0.38 mmol, 0.004 eq) were mixed together in anhydrous THF (300 mL) and aqueous K3PO4 (100 mL of 2.0 M). To this red solution was added triethylborane (100 ml of 1.0 M in THF, 100 mmol). The solution turned black and was refluxed for 4 hours. GC/MS indicated the reaction was complete. The solution was poured into a separatory funnel and the aqueous layer separated. The organic layer was collected and solvent removed to a volume of 100 mL. Ethyl acetate/ hexanes (300 mL of 1:1) were added and the solution was extracted with 1N HCl (1×100 mL), sodium bicarbonate (2×100 mL) and brine (1×100 mL). The solution was dried over sodium sulfate and vacuum filtered through a bed of silica gel (125 ml of silica). The solvent was removed at reduced pressure to afford 20.6 grams of 11 as light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-3614edc1c4b34c95b7c0dffb015dcf6a
出典メモuspto-grants-2010_06