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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846843Generated: November 3, 2026

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

https://huagongshe.com/reaction/1846843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-benzyloxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-benzene sulfonamideHCID 86725693—
ReactantN-(5-Hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-2-methyl-benzenesulfonamideHCID 86725700—
ProductN-(5-Benzyloxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-2-methyl-benzenesulfonamideHCID 8672570140.85%

Reaction Steps

N-(5-Benzyloxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-2-methyl-benzenesulfonamide (10-02) (4.7 g, 40.85%) was synthesized as a white solid from N-(5-hydroxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-2-methyl-benzenesulfonamide (9-02) (9.0 g, 27.69 mmol) following the procedure described for N-(5-benzyloxy-6-hydroxymethyl-4-oxo-4H-pyran-2-ylmethyl)-benzenesulfonamide (10-01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952039B2
Source datasetuspto-grants-2015_02
ORD IDord-f178b942107f4841bbc1d8b99739e2bb
Source noteuspto-grants-2015_02