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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52573Generated: October 26, 2026

Water → 3-Bromo-5-ethoxypyridine

https://huagongshe.com/reaction/52573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 19963750HCID 19963750—
SolventDiethyl EtherHCID 3283—
Product3-Bromo-5-ethoxypyridineHCID 1229348017.9%

Reaction Conditions

Temperature65 °C

Reaction Steps

1,5-Dibromopyridine (98%) was purchased from Lancaster Chemical Company. Sodium ethoxide (96%) and N,N-dimethylformamide (DMF) (99.9+ %. HPLC grade) were purchased from Aldrich Chemical Company. Under a nitrogen atmosphere, a mixture of3,5-dibromopyridine (5.00 g, 21.1 mmol). sodium ethoxide (2.87 g, 42.2 mmol), and DMF (10 mL) was stirred and heated at 65° C. for 15 h. The mixture was poured into water (70 mL), and anhydrous diethyl ether (155 mL) was added. Because of insoluble solids, it was necessary to filter both phases. The aqueous layer was separated and extracted with ether (2 ×25,3 ×50 mL). The combined ether extracts were dried (MgSO4), filtered, and concentrated by rotary evaporation, producing a dark-brown syrup. The brown residue was purified by vacuum distillation, affording 0.76 g (17.9%) of an oil, bp 105° C. at 5 mm Hg. 1HNMR(CDCl3): δ 9.12 (br s, 1H), 8.83 (br s, 1H), 8.42 (dd, 1H), 4.41(q,2H), 1.42(t, 3H). 13C NMR (CDCl3): δ 142.72, 136.50. 1.23.78. 64.31.14.:57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616716
Source datasetuspto-grants-1997_04
ORD IDord-13c59c91bb914cb3a3a9d30aae7e839b
Source noteuspto-grants-1997_04