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HRID 1159作成日:2026年10月25日

2-(4-(4-Hydroxy-1-butenyl)phenyl)-5-decyloxypyrimidine → 2-(4-(4-Hydroxybutyl)-phenyl)-5-decyloxypyrimidine

https://huagongshe.com/reaction/1159

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-(4-Hydroxy-1-butenyl)phenyl)-5-decyloxypyrimidineHCID 54459343—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-(4-Hydroxybutyl)-phenyl)-5-decyloxypyrimidineHCID 1969490099%

反応手順

0.38 g (1 mmol) of the thus obtained 2-(4-(4-hydroxy-1-butenyl) phenyl)-5-decyloxypyrimidine was dissolved in 20 ml of tetrahydrofuran, added with 0.05 g of 10% Pd/C and subjected to a hydrogenation reaction in a hydrogen atmosphere under normal pressure. The reaction was stopped when about 25 ml of hydrogen was consumed. Then 10% Pd/C was filtered out and the filtrate was concentrated to obtain 0.38 g of 2-(4-(4-hydroxybutyl)-phenyl)-5-decyloxypyrimidine (yield: 99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723610
出典データセットuspto-grants-1998_03
ORD IDord-b9c7d389a33241bbb79d7412a80e13bc
出典メモuspto-grants-1998_03