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HRID 322871作成日:2026年10月25日

Triphenylphosphine → methyl (RS)-5-[3-(3-methyl-2-thienylmethoxy)phenyl]-4-(2-methylphenyl)-5-oxopentanoate

https://huagongshe.com/reaction/322871

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
反応物methyl (RS)-5-(3-hydroxyphenyl)-5-oxo-4-(2-methylphenyl)pentanoateHCID 10805064—
反応物(3-Methylthiophen-2-yl)methanolHCID 12875263—
溶媒TetrahydrofuranHCID 8028—
生成物methyl (RS)-5-[3-(3-methyl-2-thienylmethoxy)phenyl]-4-(2-methylphenyl)-5-oxopentanoateHCID 2320427738.6%

反応条件

温度5 °C

反応手順

A solution of triphenylphosphine (1.13 g) in tetrahydrofuran (30 mL) is treated with diisopropyl azodicarboxylate (0.84 mL) at 0-5° C. The suspension is then treated with methyl (RS)-5-(3-hydroxyphenyl)-5-oxo-4-(2-methylphenyl)pentanoate (671 mg) and 3-methyl-2-thienylmethanol (275 mg), and stirred at 5° C. for 15 minutes. The solution is evaporated and the residue is subjected to flash chromatography on silica gel, eluting with a mixture of pentane and ethyl acetate (5:1 v/v), to give methyl (RS)-5-[3-(3-methyl-2-thienylmethoxy)phenyl]-4-(2-methylphenyl)-5-oxopentanoate (350 mg), in the form of an oil. [NMR(CDCl3):- 2.0-2.5(4H,m), 2.25(3H,s),2.5(3H,s), 3.65(3H,s), 4.8(1H,m),5.1 (2H,q),6.85-7.5(10H)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211234B1
出典データセットuspto-grants-2001_04
ORD IDord-7d6ff9da47ce431188d4f1f50ec7c1a9
出典メモuspto-grants-2001_04