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HRID 327989作成日:2026年10月25日

2-[6-(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)-5-hexynyloxy]benzenepropanoic acid methyl ester → 2-[6-(3,4-Dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)hexyloxy]benzenepropanoic acid methyl ester

https://huagongshe.com/reaction/327989

反応式

関与物質

役割名称HCID仕込み量
反応物2-[6-(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)-5-hexynyloxy]benzenepropanoic acid methyl esterHCID 53963375—
溶媒MethanolHCID 887—
生成物2-[6-(3,4-Dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)hexyloxy]benzenepropanoic acid methyl esterHCID 5403162486%

反応手順

Catalytic hydrogenation of 2-[6-(3,4-Dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)-5-hexynyloxy]benzenepropanoic acid methyl ester in methanol was carried out using the procedure of example 51. 2-[6-(3,4-Dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)hexyloxy]benzenepropanoic acid methyl ester was obtained as a colorless oil, in 86% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05273999
出典データセットuspto-grants-1993_12
ORD IDord-3dfcb9f878ca4df0ba79ae8690416fdb
出典メモuspto-grants-1993_12