Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383017Generated: October 29, 2026

Diethylamine → HCID 14372173, compound

https://huagongshe.com/reaction/1383017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantOxalyl chlorideHCID 65578—
ReactantFuro[2,3-b]pyridine-5-carboxylic acidHCID 14372168—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 14372173HCID 14372173124.5%

Reaction Steps

To a suspension of furo[2,3-b]pyridine-5-carboxylic acid (3.30 g, 20.2 mmol) in methylene chloride (80 mL), under a nitrogen atmosphere at room temperature, was added oxalyl chloride (4.2 mL, 48 mmol) and then four drops of dimethylformamide. The reaction mixture was stirred until gas evolution ceased (4-5 hours) and a clear solution resulted. This solution was evaporated in vacuo and the excess oxalyl chloride chased by evaporation with benzene. The residue was dissolved in chloroform (50 mL) and diethylamine (5.2 mL, 50 mmol) was added carefully. After 0.5 hours, the chloroform solution was washed with dilute hydrochloric acid, filtered through a pad of charcoal and evaporated to give crude product (5.49 g). This oil was distilled under vacuum to give purified product (3.62 g, 82% yield), bp: 168°-170° C./1.6 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808595
Source datasetuspto-grants-1989_02
ORD IDord-fc6eda01c23148029ba41eacf5c7f6bd
Source noteuspto-grants-1989_02