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HRID 902465作成日:2026年10月26日

3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl ester → 4-Hydroxyimino-tetrahydro-thiophene-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/902465

反応式

関与物質

役割名称HCID仕込み量
反応物3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl esterHCID 98424—
反応物Hydroxyamine hydrochlorideHCID 443297—
生成物4-Hydroxyimino-tetrahydro-thiophene-3-carboxylic acid methyl esterHCID 73675276—

反応手順

Compounds of structure (II) were prepared by using 4-amino-thiophene-3-carboxylic acid methyl ester, as depicted by formula (21), as a starting material. To make this compound, methyl thioglycolate was reacted with methyl acrylate to yield intermediate 3-methoxycarbonylmethylsulfanyl-propionic acid methyl ester, depicted by formula (18), which was cyclized to 4-oxo-tetrahydro-thiophene-3-carboxylic acid methyl ester, depicted by formula (19). This intermediate was reacted with hydroxylamine hydrochloride to yield 4-hydroxyimino-tetrahydro-thiophene-3-carboxylic acid methyl ester, depicted by formula (20), which yielded 4-amino-thiophene-3-carboxylic acid methyl ester hydrochloride, depicted by formula (21), as shown in Scheme 10.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07365200B2
出典データセットuspto-grants-2008_04
ORD IDord-d591ede4f62046339552f194d440be9b
出典メモuspto-grants-2008_04