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3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl ester → 4-Hydroxyimino-tetrahydro-thiophene-3-carboxylic acid methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl ester | HCID 98424 | — |
| 反応物 | Hydroxyamine hydrochloride | HCID 443297 | — |
| 生成物 | 4-Hydroxyimino-tetrahydro-thiophene-3-carboxylic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07365200B2 |
| 出典データセット | uspto-grants-2008_04 |
| ORD ID | ord-d591ede4f62046339552f194d440be9b |
| 出典メモ | uspto-grants-2008_04 |