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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931213Generated: October 30, 2026

HCID 178522995, compound → 5-benzyloxy-N-(4-fluoro-benzyl)-6-formyl-4-hydroxy-nicotinic acid amide

https://huagongshe.com/reaction/1931213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178522995HCID 178522995—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product5-benzyloxy-N-(4-fluoro-benzyl)-6-formyl-4-hydroxy-nicotinic acid amideHCID 17851998484.2%

Reaction Steps

After manganese dioxide (49 g) was added to a suspension of the compound 10 (9.8 g, 25.6 mmol) in chloroform (490 ml), the mixture was stirred at room temperature for 1 hour. After the reaction solution was stirred at 60° C. for 20 minutes, Celite filtration was performed, and this was washed with chloroform heated at 50° C. The filtrate was distilled off under reduced pressure to obtain 5-benzyloxy-N-(4-fluoro-benzyl)-6-formyl-4-hydroxy-nicotinic acid amide 12 (8.2 g, 84%) as a pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188271B2
Source datasetuspto-grants-2012_05
ORD IDord-7ac07432362e4677b2dda02dd377996b
Source noteuspto-grants-2012_05