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HRID 2390106作成日:2026年10月25日

Ethyl Acetate → Tert-butyl(4-chloro-2-ethynylphenoxy)acetate

https://huagongshe.com/reaction/2390106

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Tetrabutylammonium Fluoride TrihydrateHCID 11726816—
反応物Tert-butyl{4-chloro-2-[(trimethylsilyl)ethynyl]phenoxy}acetateHCID 56594380—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—

反応手順

A solution of tert-butyl{4-chloro-2-[(trimethylsilyl)ethynyl]phenoxy}acetate (Intermediate 2, 17.70 g; 52.2 mmol) in THF (180 mL) was treated with tetrabutylammonium fluoride trihydrate (16.48 g; 52.2 mmol). The reaction mixture was stirred for 4 hours, then ethyl acetate (450 mL) was added and the organic phase was washed with water (750 mL) then with brine (750 mL), dried over MgSO4, filtered and concentrated under vacuum to give a brown oily residue which was purified by flash chromatography (silica) eluting with cyclohexane containing increasing amounts of ethyl acetate. The title compound was obtained as a brown oil which solidified after prolonged standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08273769B2
出典データセットuspto-grants-2012_09
ORD IDord-b18812189ce24d5c8731b2516ed810b4
出典メモuspto-grants-2012_09