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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347814Generated: November 1, 2026

Dimethylformamide → Ethyl 2-azabicyclo[2.2.1]heptane-3-carboxylate

https://huagongshe.com/reaction/347814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 21084198HCID 21084198—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-azabicyclo[2.2.1]heptane-3-carboxylateHCID 13258847—

Reaction Steps

To a solution of 2-(4-methoxybenzyl)-2-azabicyclo[2.2.1]heptane-3-carboxylic acid (297 mg, 1.14 mmol) in dichloromethane (4.4 ml) were added oxalyl chloride (0.21 ml, 2.34 mmol) and N,N-dimethylformamide (0.09 ml, 1.14 mmol) while being cooled with ice, and the mixture was stirred at room temperature for 30 minutes. Separately, to a suspension of hydroxylamine hydrochloride (316 mg, 4.55 mmol) in tetrahydrofuran (1.5 ml)-water (0.3 ml) was added triethylamine (0.97 ml, 6.94 mmol) at 0° C., and the mixture was stirred at 0° C. for 15 minutes. To this reaction mixture was added the acid chloride solution at 0° C., and the mixture was stirred at room temperature for 15 hours. The reaction mixture, with water added thereto, was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated and the resulting residue was purified by silica gel column chromatography (2% methanol/chloroform), to give the entitled compound (152 mg, 47% through the two steps of (b) and (c)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176217B2
Source datasetuspto-grants-2007_02
ORD IDord-994af23da4b247e4b60621db5166a6f8
Source noteuspto-grants-2007_02