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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178515448 | HCID 178515448 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 6-bromo-2H-[1,3]dioxolo[4,5-b]pyridine | HCID 12563090 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09050327B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-3376832106884685b79edc450f2bd8e8 |
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| Source note | uspto-grants-2015_06 |
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