HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844161Generated: October 30, 2026
Bromine → 3-(Benzyloxy)-5-bromopyridin-2-amine
https://huagongshe.com/reaction/1844161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Amino-3-benzyloxypyridine | HCID 90334 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Benzyloxy)-5-bromopyridin-2-amine | HCID 20626554 | — |
Reaction Steps
200 g (1 mol) of 2-amino-3-benzyloxypyridine were initially charged in 4 l of dichloromethane, and a solution of 62 ml (1.2 mol) of bromine in 620 ml of dichloromethane was added at 0° C. over a period of 30 min. After the addition had ended, the reaction solution was stirred at 0° C. for 60 min. About 4 l of saturated aqueous sodium bicarbonate solution were then added to the mixture. The organic phase was separated off and concentrated. The residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate 6:4), and the product fractions were concentrated. This gave 214 g (77% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946215B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-0fa88b2e9ad7498e967972674709df92 |
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| Source note | uspto-grants-2015_02 |
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