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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846849Generated: October 30, 2026

N-(5-hydroxy-4-oxo-4H-pyran-2-ylmethyl)-benzene sulfonamide → 2-Chloro-N-(5-hydroxy-4-oxo-4H-pyran-2-ylmethyl)-benzenesulfonamide

https://huagongshe.com/reaction/1846849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-hydroxy-4-oxo-4H-pyran-2-ylmethyl)-benzene sulfonamideHCID 86725691—
ReactantN-(5-Benzyloxy-4-oxo-4H-pyran-2-ylmethyl)-2-chloro-benzenesulfonamideHCID 86725707—
Product2-Chloro-N-(5-hydroxy-4-oxo-4H-pyran-2-ylmethyl)-benzenesulfonamideHCID 8672570874%

Reaction Steps

2-Chloro-N-(5-hydroxy-4-oxo-4H-pyran-2-ylmethyl)-benzenesulfonamide (8-03) (15.0 g, crude) was synthesized as a light brown solid from N-(5-benzyloxy-4-oxo-4H-pyran-2-ylmethyl)-2-chloro-benzenesulfonamide (7-03) (26.0 g, 64.19 mmol) following the procedure described for N-(5-hydroxy-4-oxo-4H-pyran-2-ylmethyl)-benzenesulfonamide (8-01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952039B2
Source datasetuspto-grants-2015_02
ORD IDord-19d8220306224f299449f70a86c905c2
Source noteuspto-grants-2015_02