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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296030Generated: October 30, 2026

Triphenylphosphine → 4-(Aminomethyl)-5-bromo-2-ethoxy-N-methylbenzamide

https://huagongshe.com/reaction/1296030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 22929709HCID 22929709—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(Aminomethyl)-5-bromo-2-ethoxy-N-methylbenzamideHCID 22929731104.7%

Reaction Steps

After dissolving the N1-methyl-4-(azidomethyl)-5-bromo-2-ethoxybenzamide (5.32 g) in tetrahydrofuran (50 ml) and water (3 ml), triphenylphosphine (5.4 g) was added and the mixture was stirred at room temperature for 4 days. The reaction mixture was concentrated and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (5.11 g) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-4fc77f5f4b9f41d2bcc28223c4f7a922
Source noteuspto-grants-2007_07