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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099496Generated: November 1, 2026

Diisopropylamine → 2-(7-Methoxy-1-naphthyl)-2-oxoacetamide

https://huagongshe.com/reaction/1099496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
Reactant(7-Methoxy-1-naphthyl)(oxo)acetic acidHCID 14462720—
ReactantPropylphosphoric anhydrideHCID 16167369—
SolventAcetonitrileHCID 6342—
Product2-(7-Methoxy-1-naphthyl)-2-oxoacetamideHCID 4462857480%

Reaction Steps

In a reactor, 1 g of the compound obtained in Step A is introduced into 30 ml of acetonitrile, and there are then added 4.39 g of propylphosphonic anhydride and 438 mg of NH4Cl and, at the end of the addition, 3.8 ml of diisopropylamine at ambient temperature. The solution is stirred for 4 hours under nitrogen, the solvents are then evaporated off, the residue is taken up in saturated aqueous NaCl solution, and extraction with ethyl acetate is carried out. The solvents are then dried over Na2SO4 and then evaporated off to yield the title product in the form of an orange solid in a yield of 80% and with a chemical purity of 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143449B2
Source datasetuspto-grants-2012_03
ORD IDord-76d24fd61dce4e10a5841825c1b5b095
Source noteuspto-grants-2012_03