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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860623Generated: November 1, 2026

Toluene → 5-Bromobenzofuran-2-carboxylic Acid Diethylamide

https://huagongshe.com/reaction/1860623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiethylamineHCID 8021—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromobenzo[b]furan-2-carbonyl chlorideHCID 2795534—
SolventWaterHCID 962—
Product5-Bromobenzofuran-2-carboxylic Acid DiethylamideHCID 994810688%

Reaction Steps

1.3 g. of 5-bromobenzofuran-2-carbonyl chloride, 1 mL [sic] of ethyldiisopropylamine and 30 mL [sic] of toluene are mixed and 0.62 ml of diethylamine is added to the brown-coloured solution with stirring. A precipitate is formed with a slightly exothermic reaction. After 5 minutes, the mixture was treated with 30 ml of completely deionized water and the phases were separated. The organic phase was washed with 1.) 20 ml of iN HCl 2.) 20 ml of iN NaOH 3.) 20 ml of water and then with 20 ml of saturated NaCl solution and then freed of solvent components in vacuo. After chromatography on silica gel the residual, yellowish oil forms in the eluent MtB ether/heptane 2:1 [sic]. Final weight: 1.3 g of colourless crystals [sic] (yield: 88%), m.p. 79-81°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531503B1
Source datasetuspto-grants-2003_03
ORD IDord-e9a61a07ea404af9b3049a840a309c3b
Source noteuspto-grants-2003_03