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HRID 1971作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Bromothymol BlueHCID 6450—
反応物BenzylamineHCID 7504—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物Tetraethyl 3-oxopentane-1,1-bisphosphonateHCID 12499407—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物Tetraethyl 3-benzylaminopentane-1,1-bisphosphonateHCID 19689047—

反応手順

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.

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-ea7684e9a71040288dbea5e299a3c7d7
出典メモuspto-grants-1998_03