HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380777Generated: November 4, 2026
Ammonia → Methyl 4-aminothiophene-3-carboxylate
https://huagongshe.com/reaction/2380777
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | 3-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl ester | HCID 98424 | — |
| Product | Methyl 4-aminothiophene-3-carboxylate | HCID 2777610 | — |
Reaction Steps
Diazotization of methyl 4-aminothiophene-3-carboxylate with sodium nitrite followed by treatment with dimethylamine provides methyl 4-[(dimethylamino)diazenyl]thiophene-3-carboxylate. Treatment of the ester with ammonia gave the required 4-[dimethylamino)diazenyl]thiophene-3-carboxamide (compd. No. 13). The methyl 4-aminothiophene-3-carboxylate is produced using known procedures in the prior art (33, 34, 35). Thus addition of methyl acrylate to methyl thioglycolate provided methyl 3-[(methoxycarbonyl)methylthio]propanoate in quantitative yield, which on cyclization in presence of sodium methoxide gave methyl 4-oxo-2,3,5-trihydrothiophene-3-carboxylate. Treatment of methyl 4-oxo-2,3,5-trihydrothiophene-3-carboxylate with hydroxylamine followed by basification with ammonia gave methyl 4-aminothiophene-3-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258119B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-b8422c6e9b4748fc896b3462859076a5 |
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| Source note | uspto-grants-2012_09 |
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