HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895883Generated: October 29, 2026
Bromine → 3-Bromo-5-chloropyridin-2-amine
https://huagongshe.com/reaction/895883
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Amino-5-chloropyridine | HCID 66174 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Bromo-5-chloropyridin-2-amine | HCID 2763971 | 48.2% |
Reaction Steps
A suspension of 2-amino-5-chloropyridine (5.14 g, 40 mmol) and anhydrous sodium acetate (3.29 g, 40 mmol) in acetic acid (25 mL) was mechanically stirred and warmed to a bath temperature of 45° C. A solution of bromine (2.1 mL, 40 mmol) in acetic acid (2 mL) was added over 1 hour. The resulting orange mixture was cooled to 15° C. and filtered. The solids were taken up in 400 mL of water, the suspension made basic by addition of 1 N NaOH and the suspension extracted with ethyl acetate (5×100 mL). The combined extracts were washed with 10% NaHSO3 (1×100 mL) and were dried over MgSO4. Concentration afforded 2-amino-3-bromo-5-chloropyridine (4 g, 48), mp 82-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06916933B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-490f70234edd41dfb87b56b236f4b919 |
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| Source note | uspto-grants-2005_07 |
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