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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846874Generated: November 1, 2026

N-(5-hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-benzene sulfonamide → N-(5-Hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-4-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1846874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-benzene sulfonamideHCID 86725692—
ReactantN-(5-Hydroxy-4-oxo-4H-pyran-2-ylmethyl)-4-methyl-benzenesulfonamideHCID 86725731—
ProductN-(5-Hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-4-methyl-benzenesulfonamideHCID 8672573245.34%

Reaction Steps

N-(5-Hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-4-methyl-benzenesulfonamide (9-06) (7.0 g, 45.34%) was synthesized as a white solid from N-(5-hydroxy-4-oxo-4H-pyran-2-ylmethyl)-4-methyl-benzenesulfonamide (8-06) (14.0 g, 47.45 mmol) following the procedure described for N-(5-hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-benzenesulfonamide (9-01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952039B2
Source datasetuspto-grants-2015_02
ORD IDord-420fb92b199a4a3490ac681cbf734808
Source noteuspto-grants-2015_02