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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170036Generated: October 27, 2026

Dibromomethane → 6-bromo-2H-[1,3]dioxolo[4,5-b]pyridine

https://huagongshe.com/reaction/2170036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178515448HCID 178515448—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product6-bromo-2H-[1,3]dioxolo[4,5-b]pyridineHCID 12563090—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a suspension of 5-Bromo-pyridine-2,3-diol (10.0 g, 52.63 mmol, commercially available, CAS 34206-49-0) in NMP (100 mL) was added K2CO3 (21.97 g, 158 mmol) and dibromo methane (10.97 g, 63.16 mmol). The reaction mixture was heated to 90° C. for 16 h. EtOAc was added and the salts were filtered off. Water was added, the phases were separated and the aq layer was extracted with more ethyl acetate. The combined organic layers was dried over anhydrous Na2SO4 and concentrated under vacuo to get the crude compound. The crude compound was purified by silica gel chromatography (eluent 5% ethyl acetate in petrol ether). Yield of 6-Bromo-[1,3]dioxolo[4,5-b]pyridine 2.2 g (21%) pure by 1H NMR (400 MHz, DMSO) δ 7.71 (d, 1H, J=2 Hz), 7.55 (d, 1H, J=2 Hz), 6.20 (s, 2H). Mp 69-71 C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050327B2
Source datasetuspto-grants-2015_06
ORD IDord-3376832106884685b79edc450f2bd8e8
Source noteuspto-grants-2015_06