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HRID 41444作成日:2026年10月25日

Tetrahydrofuran → 5-Isopropenyl-2,4-dimethoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/41444

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Cesium carbonateHCID 10796—
反応物Methyl 5-bromo-2,4-dimethoxybenzoateHCID 3859236—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物5-Isopropenyl-2,4-dimethoxy-benzoic acid methyl esterHCID 59263148—

反応手順

To potassium isopropylidene trifluoroborate (4.87 g, 32.7 mmol) and 5-bromo-2,4-dimethoxybenzoic acid methyl ester (7.5 g, 27.3 mmol) in THF (195 ml) was added Cs2CO3 (26.6 g, 81.8 mmol) in water (39 ml). The reaction was degassed and Pd(PPh3)4 (1.58 g, 1.36 mmol) added. The reaction was heated at reflux for three days then quenched by adding water and extracted with EtOAc (×2). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated to leave an orange solid. The product was taken up in EtOAc again and the precipitate filtered. The filtrate was evaporated to dryness to yield 5-isopropenyl-2,4-dimethoxy-benzoic acid methyl ester (6.2 g). 1H NMR (Me-d3-OD) 7.68 (1H, s), 6.66 (1H, s), 5.10-5.08 (1H, m), 5.02-5.00 (1H, m), 3.93 (3H, s), 3.92 (3H, s), 3.84 (3H, s), 2.08-2.06 (3H, m). MS: [M+H]+ 237.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530469B2
出典データセットuspto-grants-2013_09
ORD IDord-ffbebf3f17d54c9a9a80f76eb51f7824
出典メモuspto-grants-2013_09