戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1451497作成日:2026年10月26日

Sodium hydride → (R)-1-(2-(2-benzylbenzyloxy)ethyl)-3-piperidinecarboxylic acid ethyl ester

https://huagongshe.com/reaction/1451497

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-Benzylbenzyl alcoholHCID 74109—
反応物(R)-1-(2-bromoethyl)nipecotic acid ethyl ester hydrobromideHCID 70009171—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-1-(2-(2-benzylbenzyloxy)ethyl)-3-piperidinecarboxylic acid ethyl esterHCID 541124588.4%

反応手順

Sodium hydride (2.1 g, 53 mmol, 60% oil dispersion) was added portionwise to a stirred solution of 2-benzylbenzylalcohol (5.0 g, 25 mmol) in dry THF (125 ml) placed under an atmosphere of nitrogen. The mixture was heated at reflux for 1 h and then allowed to cool to ambient temperature within 30 minutes. (R)-1-(2-Bromoethyl)-3-piperidinecarboxylic acid ethyl ester hydrobromide (8.6 g, 25 mmol, EP 374801) was added and the mixture was stirred for 2 days at ambient temperature. The reaction mixture was diluted with THF (100 ml) and filtered. The solvent was evaporated in vacuo to give an oily residue which was purified by column chromatography (700 g, heptane/ethyl acetate=1/1) to give 0.8 g of (R)-1-(2-(2-benzylbenzyloxy)ethyl)-3-piperidinecarboxylic acid ethyl ester as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05604242
出典データセットuspto-grants-1997_02
ORD IDord-d6f6c692759448d6b8358f840d6520db
出典メモuspto-grants-1997_02