HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476767Generated: October 30, 2026
Hydrogen Bromide → 5-Bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine
https://huagongshe.com/reaction/1476767
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 7-Fluoro-2,3-dihydro-1,4-benzodioxin-5-amine | HCID 66680600 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine | HCID 89635954 | — |
Reaction Steps
NaNO2 (2.69 g, 39.9 mmol) in water (20 mL) was added slowly at 0° C. to a solution of 7-fluoro-2,3-dihydrobenzo[b][1,4]dioxin-5-amine (4.5 g, 26 mmol) in aq.47% HBr (20 mL) and continued stirring at same temperature for 30 min. The above diazonium salt solution was added slowly to a solution of CuBr (5.7 g, 39.9 mmol) in aq.47% HBr (25 mL) at 0° C. and stirred at 25° C. for 30 min. Reaction mixture was quenched with ice water, extracted with ethyl acetate (3×50 mL), washed it with water followed by brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford crude. The crude was purified by column purification (using silica gel and 0-5% ethyl acetate in Hexane as eluent) to afford 5-bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine (Int-53) (5.9 g). 1H NMR (300 MHz, CDCl3) δ ppm 6.9-6.84 (1H, dd), 6.6-6.5 (1H, dd), 4.3-4.3 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09402833B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-759071f72133440188873ed5c99f1a60 |
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| Source note | uspto-grants-2016_08 |
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