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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073979Generated: October 30, 2026

Bromine → HCID 13849603, compound

https://huagongshe.com/reaction/2073979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodium AcetateHCID 517045—
ReactantHCID 13849602HCID 13849602—
SolventDichloromethaneHCID 6344—
ProductHCID 13849603HCID 13849603—

Reaction Steps

Sodium acetate (2.40 g, 0.0292 mol) and bromine (7.5 mL, 0.146 mol) are added to a solution of diethyl 3-bromofuro[2,3-b]pyridine-5,6-dicarboxylate (5.00 g, 0.0146 mol) in methylene chloride (150 mL). The mixture is stirred at room temperature for four days then washed with aqueous sodium bisulfate to remove unreacted bromine. The aqueous solution is then back extracted with methylene chloride. The organic solution is combined, dried over sodium sulfate and filtered. To the filtrate is added 1,8-diazabicyclo-[5.4.0]undec-7-ene (4.4 mL, 0.032 mol), and the mixture is stirred at room temperature for one hour. The solution is then concentrated in vacuo. The residue is chromatographed over silica gel eluting with 20% ethyl acetate in hexane, yielding the crude 2,3-dibromofuro[2,3-b]pyridine as a white solid in 95% yields recrystallization from a methylene chloride-hexane mixture affords diethyl 2,3-dibromofuro[2,3-b]pyridine-5,6-dicarboxylate mp 96°-98° C. in 75.9% recrystallized yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920226
Source datasetuspto-grants-1990_04
ORD IDord-d4b9f30171cb46018feea630b9dcf23e
Source noteuspto-grants-1990_04