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HRID 2189747作成日:2026年10月26日

Tetrahydrofuran → Ethyl 3-chloro-4-(2-methylpropyl)benzoate

https://huagongshe.com/reaction/2189747

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Ethyl 4-bromo-3-chlorobenzoateHCID 12594301—
反応物HCID 178448254HCID 178448254—
生成物Ethyl 3-chloro-4-(2-methylpropyl)benzoateHCID 59316731—

反応手順

A solution of isobutylzinc bromide in THF (0.5 M, 30 mL, 15.0 mmol) was added under argon to ethyl 4-bromo-3-chlorobenzoate (D16) (2.00 g, 7.60 mmol) and then 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane complex (930 mg, 1.14 mmol) was added. The reaction was heated to reflux for 4.5 h. The mixture concentrated in vacuo and the residue partitioned between ethyl acetate (125 mL) and water (125 mL). A solid formed, which was filtered off and discarded. The organic layer was washed with water (100 mL), dried (phase separator) and concentrated in vacuo. The crude product was purified by silica chromatography, eluting with 0-5% EtOAc in hexane over 30 minutes to give the title compound as a colourless oil (1.76 g, 7.33 mmol). δH (d6-DMSO, 400 MHz): 7.91 (1H, d), 7.80 (1H, dd), 7.46 (1H, d), 4.30 (2H, q), 2.66 (2H, d), 1.88-2.01 (1H, m), 1.32 (3H, t), 0.89 (6H, d).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08324254B2
出典データセットuspto-grants-2012_12
ORD IDord-e097eab6fd8141a5a56cf02e82c39a73
出典メモuspto-grants-2012_12