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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451311Generated: November 1, 2026

Dichloromethane → HCID 10487090, compound

https://huagongshe.com/reaction/1451311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-Furoic acidHCID 10268—
ReactantOxalyl chlorideHCID 65578—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
CatalystPyridineHCID 1049—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
ProductHCID 10487090HCID 1048709088.7%

Reaction Steps

To a suspension of furan-3-carboxylic acid (36 g, 0.32 mol) in 250 ml of toluene was added 49 g (0.385 mol) of oxalyl chloride and 1 drop of pyridine, and the mixture was heated at 80°-90° C. for 1.5 h. The mixture was cooled to room temperature, N,O-dimethylhydroxylamine hydrochloride (35 g, 0.36 mol), 4-dimethylaminopyridine (DMAP, 1.8 g, 0.0147 mol), and 600 ml of methylene chloride were added. The mixture was cooled to 0° C., 68.4 g of pyridine was added slowly, the mixture was allowed to warm to room temperature and stirred for 2 h. The mixture was filtered, and the filtrate was washed with water, 5% aqueous dimethylaminopropylamine, water, 6N HCl solution, water, and brine. The organic layer was dried and concentrated in vacuo, and the residue was distilled (b.p. 85°-87° C./0.2 mm) to afford 44 g (88.7%) of 3-(N-methyl-N-methoxycarbamoyl)furan.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604224
Source datasetuspto-grants-1997_02
ORD IDord-02117c5d03e641a2afb20aa6412b7009
Source noteuspto-grants-1997_02