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HRID 1974作成日:2026年10月23日

Benzoyl chloride → tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonate

https://huagongshe.com/ja/reaction/1974

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物TriethylamineHCID 8471—
反応物Tetraethyl 5-aminopentane-1,1-bisphosphonateHCID 12102991—
溶媒DichloromethaneHCID 6344—
生成物tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonateHCID 1968903130.7%

反応手順

A solution of benzoyl chloride (0.73 g, 5.0 mmol) in dichloromethane was added slowly to a solution of tetraethyl 5-aminopentane-1,1-bisphosphonate (1.50 g, 4.5 mmol) from Example 11, part A, and triethylamine (0.76 mL, 5.5 mmol) in dichloromethane at 0° C. After warming to room temperature for 30 minutes, the reaction was quenched by addition of 1N HCl (30 mL). The product was extracted into dichloromethane (2×20 mL) and the combined organic layers were washed with saturated NaHCO3 (2×15 mL), dried (Na2SO4), and concentrated in vacuo. Flash chromatography on silica gel eluting with 15% i-propanol in ethylacetate in EtOAc gave the title compound (0.64 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728650
出典データセットuspto-grants-1998_03
ORD IDord-18119a89941c4368a7ad288ebe54d59f
出典メモuspto-grants-1998_03