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HRID 218057作成日:2026年10月26日

Sodium hydride → Diethyl 2-allyl-2-iodomalonate

https://huagongshe.com/reaction/218057

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Diethyl allylmalonateHCID 74900—
反応物N-IodosuccinimideHCID 120273—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Diethyl 2-allyl-2-iodomalonateHCID 10990994—

反応手順

Following the method of Flynn and Zabrowski, J. Org. Chem. 55: 3673-3674 (1990), such reference herein incorporated by reference with regard to such synthetic teaching, diethyl allylmalonate (18.0 g, 90.0 mmol) was dissolved in tetrahydrofuran (THF) (50 mL). Sodium hydride (11.5 g, 288 mmol, 60% dispersion in oil) was added to the reaction. After 30 min of stirring at ambient temperature, a solution of N-iodosuccinimide (21.9 g, 97.2 mmol) in THF (100 mL) was added, and the reaction was stirred in the dark at ambient temperature for 15 min. The reaction was poured onto 100 g of silica gel. The contents were diluted with 400 mL of ether and stirred with a glass rod. The contents were then filtered through a bed of silica gel (100 g) in a sintered funnel. The silica gel was washed with ether (4×400 mL). The combined filtrates were concentrated by rotary evaporation to give diethyl 2-allyl-2-iodomalonate, as a yellowish orange liquid, that was used immediately in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198296B2
出典データセットuspto-grants-2012_06
ORD IDord-9b847c784fd9406c993663d282ca9b08
出典メモuspto-grants-2012_06