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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836508Generated: October 31, 2026

Dimethylamine → HCID 73855551, compound

https://huagongshe.com/reaction/1836508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 74058487HCID 74058487—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 73855551HCID 7385555150.4%

Reaction Steps

A solution [[2-(2,2-dimethyl-5-oxo-[1,3]-dioxolan-4-ylidene)-acetyl]-(4-fluorobenzyl)-aminooxy]-acetic acid (0.681 g, 1.93 mmol) in dichloromethane (20 ml) was treated at 22° C. with oxalyl chloride (0.34 ml, 3.9 mmol) and a trace of N,N-dimethylformamide and the resulting mixture was stirred for 1 h. The solvent and excess reagent were then evaporated in vacuo. The residual material was dissolved in dry dichloromethane (10 ml) and added dropwise to a cold (0° C.) solution of dimethylamine (0.18 g, 4.0 mmol) and pyridine (0.25 ml, 3.2 mmol ) in dichloromethane. After 2 h, the reaction mixture was diluted with ethyl acetate, washed with saturated sodium bicarbonate and brine and dried over anhydrous magnesium sulphate. Evaporation of the solvent in vacuo and crystallisation of the residue from a mixture of ethyl acetate and hexane gave 0.370 g (50% yield) of the title material as a white solid. 1HNMR 400 MHz (CDCl3) δ (ppm): 1.77 (6H, s, CH3), 2.91 (3H, s, CH3), 2.97 (3H, s, CH3), 4.53 (2H, s, CH2), 4.93 (2H, s, CH2), 6.43 (1H, s, CH), 7.03 (2H, m, aromatics), 7.41 (2H, m, aromatics). HRMS (ES+) calculated for C18H22FN2O6[M+H]+: 381.146190. Found: 381.146382.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777440B2
Source datasetuspto-grants-2004_08
ORD IDord-63f16f789b0e48e6b7c67eea7cc88084
Source noteuspto-grants-2004_08