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HRID 962768作成日:2026年10月27日

Hydrochloric Acid → Ethyl 4-{3-[4-(4-methylphenylmethoxy)-3-(3-chloropropoxy)benzoyl]indol-1-yl}butanoate

https://huagongshe.com/reaction/962768

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物Potassium CarbonateHCID 11430—
反応物Ethyl 4-{3-[3-hydroxy-4-(4-methylphenylmethoxy)benzoyl]indol-1-yl}butanoateHCID 19085543—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 4-{3-[4-(4-methylphenylmethoxy)-3-(3-chloropropoxy)benzoyl]indol-1-yl}butanoateHCID 1908552682.9%

反応条件

温度60 °C

反応手順

Ethyl 4-{3-[3-hydroxy-4-(4-methylphenylmethoxy) benzoyl]indol-1-yl}butanoate (2.77 g) obtained in Step 1 was dissolved in N,N-dimethylformamide (30 ml). 1-Bromo-3-chloropropane (1.39 g) and potassium carbonate (0.97 g) were added to the resultant solution and stirred for 6 hours at 60° C. The reaction mixture was poured into 2N HCl and extracted with ethyl acetate. The resultant extract was sequentially washed with saturated sodium bicarbonate solution and brine and then dried. The solvent was distilled off. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1), obtaining 2.67 g of ethyl 4-{3-[4-(4-methylphenylmethoxy)-3-(3-chloropropoxy)benzoyl]indol-1-yl}butanoate as a light yellow oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05760040
出典データセットuspto-grants-1998_06
ORD IDord-c49e09dbb9cf4c169bcb362f5e6dd098
出典メモuspto-grants-1998_06