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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259331Generated: October 29, 2026

Phosphorus oxychloride → 5-Bromo-2-chloro-3-ethoxypyridine

https://huagongshe.com/reaction/1259331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-Bromo-5-ethoxypyridineHCID 12293480—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product5-Bromo-2-chloro-3-ethoxypyridineHCID 7130367385.6%

Reaction Steps

As shown in step 2-iv of Scheme 2, phosphorous oxychloride (48.02 g, 403.6 mmol) was added to 3-bromo-5-ethoxypyridine, 1-oxide (4.4 g, 20.18 mmol) in 700 mL of DCM at RT. The reaction mixture was stirred at RT overnight. After the addition of brine, the organics were partitioned, dried over MgSO4, filtered, and the filtrate concentrated under reduced pressure. The product was purified by filtering the concentrate through a pad of silica gel and eluting the pad with ethyl acetate. The volatiles were removed under reduced pressure to provide 5-bromo-2-chloro-3-ethoxypyridine (Compound 2003, 4.3 g, 85.6%): 1H NMR (CDCl3) δ 8.1 (s, 1H), 7.32 (s, 1H), 4.15 (q, 2H), 1.6 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466288B2
Source datasetuspto-grants-2013_06
ORD IDord-71809886b30047179b1044697afd1582
Source noteuspto-grants-2013_06