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HRID 21361作成日:2026年10月26日

Acetic Acid → N-(4'-iodophenyl)-2-aminooctane

https://huagongshe.com/reaction/21361

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物1,1-DichloroethaneHCID 6365—
反応物2-OctanoneHCID 8093—
反応物4-IodoanilineHCID 10893—
反応物Sodium triacetoxyborohydrideHCID 5049666—
生成物N-(4'-iodophenyl)-2-aminooctaneHCID 992752188.2%

反応手順

A flask containing 4-iodoaniline (11.0 g, 50.2 mmol) was charged with dry dichloroethane (125 ml), 2-octanone (7.9 ml, 50.0 mmol) and sodium triacetoxyborohydride (13.8 g, 65 mmol). After stirring for 10 minutes, acetic acid (2.9 ml, 50.7 mmol) was added via syringe over a 5 minute period. The reaction was stirred under an N2 atmosphere for 16 hrs. At the end of this period the reaction was quenched by the careful addition of a solution of saturated aqueous ammonium chloride (100 ml). After stirring for 0.5 hr, the reaction was poured over ether (250 ml) and the layers were separated. The ether layer was washed with saturated aqueous ammonium chloride (100 ml), dried (Na2SO4), filtered and evaporated in vacuo. Flash column chromatography (silica, 1:39; EtOAC:hexanes) provided N-(4'-iodophenyl)-2-aminooctane (14.6 g, 88%) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05422114
出典データセットuspto-grants-1995_06
ORD IDord-c9b02b03867a4d5a8003dffb26df1f7d
出典メモuspto-grants-1995_06