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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259330Generated: November 2, 2026

Dichloromethane → 3-Bromo-5-ethoxypyridine

https://huagongshe.com/reaction/1259330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-Bromo-5-methoxypyridineHCID 817163—
Product3-Bromo-5-ethoxypyridineHCID 12293480—

Reaction Steps

As shown in step 2-iii of Scheme 2,3-chloroperoxybenzoic acid (9.426 g, 42.06 mmol) was added to 3-bromo-5-methoxypyridine (4.25 g, 21 mmol) in 200 mL of DCM at RT. The reaction was stirred overnight and the mixture was washed with 200 mL of 2 N NaOH and 2×200 mL brine. The organic phase was dried over MgSO4, filtered and the volatiles removed under reduced pressure to provide 3-bromo-5-ethoxypyridine, 1-oxide (Compound 2002, 4.4 g): 1H NMR (CDCl3): δ 8.05 (s, 1H), 7.9 (s, 1H), 7.0 (s, 1H), 4.12 (q, 2H), 1.45 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466288B2
Source datasetuspto-grants-2013_06
ORD IDord-fe35cd49bfda497e9405f4cfea5f2681
Source noteuspto-grants-2013_06