HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[5-(hydroxymethyl)-2-methyl-3-thienyl]-N-methylthiophene-2-sulfonamide → N-(5-formyl-2-methyl-3-thienyl)-N-methylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[5-(hydroxymethyl)-2-methyl-3-thienyl]-N-methylthiophene-2-sulfonamide | HCID 59411384 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(5-formyl-2-methyl-3-thienyl)-N-methylthiophene-2-sulfonamide | HCID 59411396 | 86% |
Reaction Steps
To a solution of N-[5-(hydroxymethyl)-2-methyl-3-thienyl]-N-methylthiophene-2-sulfonamide (31.1 g) in tetrahydrofuran (300 mL) was added manganese dioxide (43 g), and the mixture was stirred at room temperature overnight. The manganese dioxide was filtered off and the filtrate was concentrated and crystallized from diethyl ether to give N-(5-formyl-2-methyl-3-thienyl)-N-methylthiophene-2-sulfonamide (26.4 g, yield 86%) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492405B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-b4ba05639ba94863bf1798ca5dc10784 |
| Source note | uspto-grants-2013_07 |