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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383012Generated: October 30, 2026

Diethylamine → HCID 14372159, compound

https://huagongshe.com/reaction/1383012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantFuro[3,2-b]pyridine-6-carboxylic acidHCID 14372158—
SolventAcetoneHCID 180—
SolventChloroform waterHCID 22418719—
ProductHCID 14372159HCID 1437215996.2%

Reaction Steps

To a suspension of furo[3,2-b]pyridine-6-carboxylic acid (3.26 g, 20 mmol) in dry acetone (40 mL), under a nitrogen atmosphere and cooled in an ice bath, was added dropwise triethylamine (3.1 mL, 22.3 mmol). After 15 minutes, a solution of ethyl chloroformate (2.1 mL, 22.3 mmol) in dry acetone (12 mL) was added dropwise. This solution was stirred for two hours and then diethylamine (4.2 mL, 40.6 mmol) was added. After another hour the reaction mixture was diluted with chloroform/water and the chloroform layer separated and washed with sodium carbonate solution and then 10% hydrochloric acid. The chloroform solution was dried over anhydrous sodium sulfate, filtered through a charcoal pad and evaporated to give crude oily product (4.2 g). This material was purified by fractional distillation to give 2.42 g (55.5% yield) of oil, bp: 155°-156° C./1.2 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808595
Source datasetuspto-grants-1989_02
ORD IDord-bc9058cfbe694ba8a7387dd600211c71
Source noteuspto-grants-1989_02