HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925707Generated: October 24, 2026
Methyl 3-amino-2-thiophenecarboxylate → Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylate
https://huagongshe.com/en/reaction/1925707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-amino-2-thiophenecarboxylate | HCID 89652 | — |
| Reactant | 4-t-Butylbenzenesulfonyl chloride | HCID 139882 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylate | HCID 8015643 | 66% |
Reaction Steps
To a solution of methyl 3-aminothiophene-2-carboxylate (0.55 g; 3.5 mmol) in pyridine (2 mL) and dichloromethane (2 mL) was added 4-tert-butylbenzenesulfonyl chloride (0.98 g; 4.2 mmol). The resulting mixture was warmed to 40° C. to aid in solubility, then stirred at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane and washed with aqueous hydrochloric acid (2N). The aqueous layer was separated and extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, decanted, and filtered through a and of silica. The silica was washed with dichloromethane. The eluant was combined with hexanes and allowed to stand. After 24 hours the resulting solid product was collected by filtration to give the desired product as a white solid (817 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178699B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-4fc1342cfdfe4611b700d4c23e1bcb89 |
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| Source note | uspto-grants-2012_05 |
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