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HRID 1604233作成日:2026年10月27日

Diethyl Ether → 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide

https://huagongshe.com/reaction/1604233

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物CyclohexaneHCID 8078—
反応物Magnesium BromideHCID 82241—
反応物N-ethyl-1-naphthalenecarboxamideHCID 4088726—
反応物t-Butylperoxy benzoateHCID 21744378—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
生成物2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamideHCID 1960231933%

反応手順

A solution of 1.3M s-BuLi in cyclohexane (34 mL, 44 mmol) was added dropwise to a -78° C. cooled solution of N-ethyl-1-naphthalenecarboxamide (20 mmol) and TMEDA (6.0 mL, 40 mmol) in THF (100 mL). After 30 min, MgBr2.Et2O (15.5 g, 60 mmol) was added portion wise, and the reaction was briefly warmed to ambient temperature then was recooled to -78° C. After 1 h at -78° C., t-butylperoxy benzoate (4.3 g, 22 mmol) was added. The resulting reaction was warmed to -30° C. and worked up in the usual manner, then was purified by chromatography with 3:7 ethyl acetate/hexanes to afford 1.7 g of desired compound as a white solid, a 33% yield. m.p. 126-127° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05994270
出典データセットuspto-grants-1999_11
ORD IDord-9c54fa92272446849c5eb0d3d0b99cd6
出典メモuspto-grants-1999_11