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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453573Generated: October 29, 2026

N-[5-(hydroxymethyl)-2-methyl-3-thienyl]-N-methylthiophene-2-sulfonamide → N-(5-formyl-2-methyl-3-thienyl)-N-methylthiophene-2-sulfonamide

https://huagongshe.com/reaction/453573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[5-(hydroxymethyl)-2-methyl-3-thienyl]-N-methylthiophene-2-sulfonamideHCID 59411384—
CatalystHCID 178418406HCID 178418406—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-formyl-2-methyl-3-thienyl)-N-methylthiophene-2-sulfonamideHCID 5941139686%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492405B2
Source datasetuspto-grants-2013_07
ORD IDord-b4ba05639ba94863bf1798ca5dc10784
Source noteuspto-grants-2013_07