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HRID 592231作成日:2026年10月27日

Diethyl Ether → Tert-butyl 2-(6-chloro-5-fluoropyridin-3-yl)acetate

https://huagongshe.com/reaction/592231

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5-Bromo-2-chloro-3-fluoropyridineHCID 2763285—
反応物HCID 178451183HCID 178451183—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
触媒Ditert-butyl(cyclopenta-2,4-dien-1-yl)phosphane;iron(2+);(2,3,4,5-tetraphenylcyclopenta-1,4-dien-1-yl)benzeneHCID 129828017—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 2-(6-chloro-5-fluoropyridin-3-yl)acetateHCID 58365072—

反応条件

温度70 °C

反応手順

In a sealed tube, a mixture of 5-bromo-2-chloro-3-fluoropyridine 205-1 (631 mg, 3 mmol), 0.5 M (2-tert-butoxy-2-oxoethyl) zinc(II) chloride 205-2 in ether (6.6 mL, 3.3 mmol), Pd(dba)2 (87 mg, 0.15 mmol), 1,2,3,4,5-pentaphenyl-1′-(di-t-butylphosphino)ferrocene (Q-phos, 107 mg, 0.15 mmol), and THF (12 mL) under argon was stirred at 70° C. for 18 hours. After cooled to room temperature, the solvents were evaporated and the residue was redissolved in ethyl acetate, washed with water and brine, dried over Na2SO4 and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 30% ethyl acetate in hexane to give tert-butyl 2-(6-chloro-5-fluoropyridin-3-yl)acetate 205-3 as a brown oil. MS m/z 246.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238646B2
出典データセットuspto-grants-2016_01
ORD IDord-c79a005595ae44d6955ce647b9bd477f
出典メモuspto-grants-2016_01