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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492086Generated: October 25, 2026

Butyl Formate → 3-Fluoro-N-(5-formylaminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamide

https://huagongshe.com/reaction/492086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl FormateHCID 11614—
ReactantN-(5-aminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-3-fluoro-benzenesulfonamideHCID 57678960—
Product3-Fluoro-N-(5-formylaminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamideHCID 57678965—

Reaction Steps

A solution of 0.28 grams (0.837 mmoles) N-(5-aminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-3-fluoro-benzenesulfonamide in 6 mL n-butyl formate was heated under reflux for 1.5 hours. The solution was concentrated under reduced pressure. 3-Fluoro-N-(5-formylaminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamide was obtained by recrystallization of the residue from 2-propanol/ethyl ether to provide 0.27 grams (89%) of 3-fluoro-N-(5-formylaminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-benzenesulfonamide, m.p. 143-144° C., M+H=363

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531577B2
Source datasetuspto-grants-2009_05
ORD IDord-0241e2730b6d4ec9b84180d718e64163
Source noteuspto-grants-2009_05