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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886260Generated: October 26, 2026

Dimethylformamide → N-hydroxy-N-(1-hydroxy-2-naphthyl)-4-methoxycarbonyl-3-oxabutanamide

https://huagongshe.com/reaction/1886260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantPotassium bisulfateHCID 516920—
Reactant1-Hydroxy-2-naphthylhydroxylamine hydrochlorideHCID 85613850—
ReactantMethyl diglycolateHCID 86746156—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-hydroxy-N-(1-hydroxy-2-naphthyl)-4-methoxycarbonyl-3-oxabutanamideHCID 1987754869%

Reaction Steps

Into a 25 ml methylene chloride solution of 500 mg (3.38 mmol) of methyl diglycolate and 200 μl (3.38 mmol) of DMF was added 660 μl (7.60 mmol) of oxalyl chloride at 0° C., and the mixture was stirred as such for one hour. The mixture was added to a solution of 3.6 g (17 mmol) of 1-hydroxy-2-naphthylhydroxylamine hydrochloride, 3.5 ml (25 mmol) of triethylamine in THF (25 ml), and water (5 ml), at 0° C., and after stirring at 0° C. for one hour and at room temperature for one hour, the reaction was completed with aqueous KHSO4, and the mixture was extracted with methylene chloride. The organic layer was washed with 4N HCl and with saturated aqueous NaCl, and then dried over anhydrous magnesium sulfate, and after evaporation of the solvent under a reduced pressure, the residue was subjected to silica gel column chromatography to give 710 mg (69%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05149859
Source datasetuspto-grants-1992_09
ORD IDord-bf156d9c22174f4393ca26d80a946161
Source noteuspto-grants-1992_09