Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387767Generated: October 31, 2026

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

https://huagongshe.com/reaction/2387767

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 1003, 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 numberUS08268999B2
Source datasetuspto-grants-2012_09
ORD IDord-a3d89e1c612941009609464adbbfb457
Source noteuspto-grants-2012_09