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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1971생성일: 2026년 10월 23일

Bromothymol Blue → Tetraethyl 3-benzylaminopentane-1,1-bisphosphonate

https://huagongshe.com/ko/reaction/1971

반응식

참여 물질

역할이름HCID투입량
반응물Bromothymol BlueHCID 6450—
반응물BenzylamineHCID 7504—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Tetraethyl 3-oxopentane-1,1-bisphosphonateHCID 12499407—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물Tetraethyl 3-benzylaminopentane-1,1-bisphosphonateHCID 19689047—

반응 단계

To a stirred solution of tetraethyl 3-oxopentane-1,1-bisphosphonate (0.50 g, 1.4 mmol) in methanol (5 ml) was added a small amount of bromothymol blue and benzylamine (0.75 g, 7.0 mmol). Acetic acid was added dropwise until the solution turned yellow (pH=6), and NaCNBH3 (57 mg, 0.9 mmol) was added. The resulting yellow solution was stirred at room temperature for 2 days, at which time more NaCNBH3 (20 mg) was added. After stirring a total of 4 days, the reaction was quenched by adding concentrated HCl until the pH was less than 1, and the solvents were removed in vacuo. The residue was taken up in water (10 ml) and washed with diethyl ether (2×20 ml). The aqueous layer was made basic (pH greater than 10) by the addition of solid KOH, saturated with NaCl, and extracted with dichloromethane (5×25 ml). The combined extracts were dried (Na2SO4) and concentrated to give tetraethyl 3-benzylaminopentane-1,1-bisphosphonate. This material was hydrolyzed by heating at reflux in concentrated HCl (6 ml) for 20 hours. The volatiles were removed under vacuum, the residue dissolved in water (10 ml) and concentrated under vacuum to give 0.49 g of Compound No. 159 as a hygroscopic foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728650
출처 데이터셋uspto-grants-1998_03
ORD IDord-ea7684e9a71040288dbea5e299a3c7d7
출처 메모uspto-grants-1998_03