HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343422Generated: October 30, 2026
Benzyl Bromide → 2-(Benzyloxy)-3-bromo-5-chloropyridine
https://huagongshe.com/reaction/343422
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 178517755 | HCID 178517755 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(Benzyloxy)-3-bromo-5-chloropyridine | HCID 22058382 | — |
Reaction Steps
A mixture of 3-bromo-5-chloro-2-hydroxypyridine (81 g), benzyl bromide (52 mL) and silver carbonate (97 g)in benzene (1 L) was heated at 70° C. for 1 h. The mixture was cooled to r.t. and then filtered through a bed of celite. The filtrate was concentrated and the residual off-white solid was recrystallized from hexane to provide the title compound as a white solid (102 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861419 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-8b76334f6c4c424dbad4bf0179b242cb |
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| Source note | uspto-grants-1999_01 |
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