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HRID 1391754作成日:2026年10月26日

Tributylphosphine → Ethyl [(4-{[1-(6-bromo-2-pyridinyl)butyl]oxy}-2-methylphenyl)oxy]acetate

https://huagongshe.com/reaction/1391754

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物Ethyl (4-hydroxy-2-methylphenoxy)acetateHCID 21986458—
反応物1-(6-Bromopyridin-2-yl)butan-1-olHCID 58629859—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl [(4-{[1-(6-bromo-2-pyridinyl)butyl]oxy}-2-methylphenyl)oxy]acetateHCID 5862981735.9%

反応手順

To a stirred solution of 1-(6-bromo-2-pyridinyl)-1-butanol (626 mg, 2.72 mmol) and ethyl (4-hydroxy-2-methylphenoxy)acetate (539 mg, 2.56 mmol) in dry THF (51 mL) at 0° C. (ice/water bath) under nitrogen was added ADDM (1.32 g, 5.13 mmol) followed by nBu3P (1.28 mL, 4.95 mmol) drop-wise. The mixture was stirred with slow warming to rt over 18 hours and then concentrated under vacuum, diluted with EtOAc (150 mL) and washed with water (3×75 mL), dried (Na2SO4), filtered and reduced to give a yellow oil. Purification by SPE (silica, 20 g cartridge) eluting with cyclohexane:EtOAc (gradient 20:1 to 10:1) afforded the title compound (388 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07338960B2
出典データセットuspto-grants-2008_03
ORD IDord-bf7c010e2c6e464a9cf2cf92484e428c
出典メモuspto-grants-2008_03