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HRID 989625作成日:2026年10月27日

Water → Di-tert-butyl 2-[[[2-(benzylcarboxy)propyl]tert-butoxyphosphinyl]methyl]pentanedioate

https://huagongshe.com/reaction/989625

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzyl methacrylateHCID 17236—
反応物Sodium hydrideHCID 24758—
反応物HCID 178451016HCID 178451016—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Di-tert-butyl 2-[[[2-(benzylcarboxy)propyl]tert-butoxyphosphinyl]methyl]pentanedioateHCID 1841807453%

反応手順

To a solution of di-tert-butyl 2-[(tert-butoxy-phosphinyl)methyl]pentane-l,5-dioate (13.62 g, 36.0 mmol) and benzyl methacrylate (6.35 g, 36.0 mmol) in THF (100 ml) under nitrogen was added sodium hydride (0.14 g, 60% dispersion in oil, 3.60 mmol). After three hours, the reaction mixture was poured into water (300 ml) and ether (100 ml) was added. The organic layer was separated and retained, and the aqueous layer was washed again with ether (100 ml). The combined organic extracts were dried over magnesium sulfate and the solvent was removed under reduced pressure. The resulting residue was purified by column chromatography and the product was eluted with 2:3 EtOAc/Hexane. The solvent was removed under reduced pressure leaving a clear oil (10.5 g, 53%). 1H NMR (CDCl3) : δ 1.3 (m, 3H), 1.5 (m, 27H), 1.7 (m, 2H), 1.9 (m, 2H), 2.2 (m, 4H), 2.6 (m, 1H), 2.9 (m, 1H), 5.1 (m, 2H), 7.3 (m, 5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06458775B1
出典データセットuspto-grants-2002_10
ORD IDord-35c7d8c9469744a18055546c3631a8ae
出典メモuspto-grants-2002_10