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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1974생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1974

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물TriethylamineHCID 8471—
반응물Tetraethyl 5-aminopentane-1,1-bisphosphonateHCID 12102991—
용매DichloromethaneHCID 6344—
생성물tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonateHCID 1968903130.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728650
출처 데이터셋uspto-grants-1998_03
ORD IDord-18119a89941c4368a7ad288ebe54d59f
출처 메모uspto-grants-1998_03