5-Bromo-2-ethoxypyridine
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5-Bromo-2-ethoxypyridine
structure -
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CAS No:
55849-30-4
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Formula:
C7H8BrNO
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Chemical Name:
5-Bromo-2-ethoxypyridine
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Synonyms:
Pyridine,5-bromo-2-ethoxy-;5-Bromo-2-ethoxypyridine;3-Bromo-6-ethoxypyridine;6-Ethoxypyridin-3-yl bromide
- Categories:
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CAS No:
Characteristics
22.1
2.2
Off-white to pale yellow Solid
1.5±0.1 g/cm3
25 °C @ Solvent: Ethyl acetate
107°C/33mmHg(lit.)
218 °F
1.534
Safety Information
IRRITANT
NONH for all modes of transport
3
22-37/38-41
26-36/39
Xn,Xi
Harmful
P261-P280-P305 + P351 + P338
H302-H315-H317-H318-H335
|Danger|H302 (97.73%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P272, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P333+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 44 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
5-Bromo-2-ethoxypyridine Use and Manufacturing
Freshly cut sodium (74 mg, 3.2 mmol) was dissolved in ethanol (1.2 ml) followed by addition of 2, 5-dibromopyridine (236 mg, lmmol) in DMF (3 ml). The mixture was stirred for Ih at 8OA solution of freshly prepared sodium ethoxide (sodium, 4.9 g, 210 mmol; absolute ethanol, 100 mL, room temperature) was treated with 2, 5-dibromopyridine (10 g, 42 mmol) and was heated at reflux for 18 h. After cooling to room temperature, the mixture was poured into aqueous saturated sodium bicarbonate solution, was extracted with diethyl ether, and the ether layer was washed with brine, was dried over magnesium sulfate, was concentrated in vacuo. Purification by silica gel chromatography (100:1 hexanes-ethyl acetate) gave 7.5 g (88percent yield) of the title compound. A solution of freshly prepared sodium ethoxide (sodium, 4.9g, 210 mmol; absolute ethanol, 100 mL, room temperature) was treated with 2, 5-dibromopyridine (10g, 42 mmol) and was heated at reflux for 18 hours. After cooling to room temperature, the mixture was poured into aqueous saturated sodium bicarbonate solution, was extracted with diethyl ether, and the ether layer was washed with brine, was dried over magnesium sulfate, was concentrated in vacuo. Purification by silica gel chromatography (100:1 hexanes-ethyl acetate) gave 7.5 g (88percent yield) of the title compound. General procedure: An oven-dried Schlenk tube was charged with Pd(OAc)2 (0.015 mmol, 3.4 mg), X-Phos (0.015 mmol, 7.2 mg), Cs2CO3 (0.9 mmol, 293 mg), substrate 1 (0.3 mmol) and 2 (0.4 mmol). The reaction vessel was evacuated and backfilled again with nitrogen gas, and 1, 4-dioxane (1 mL) was added via syringe under nitrogen. The reaction mixture was stirred at 100 C for 12 hours. The reaction mixture was then cooled to room temperature and diluted with EtOAc. The crude was nextfiltered through a plug of celite, which was washed with ethyl acetate. The solution was concentrated and further purifiedby flash column chromatography to afford the corresponding product.Freshly cut sodium (74 mg, 3.2 mmol) was dissolved in ethanol (1.2 ml) followed by addition of 2, 5-dibromopyridine (236 mg, lmmol) in DMF (3 ml). The mixture was stirred for Ih at 8O0C, and cooled to rt. The reaction was quenched with water (4 mL) and extracted with ether three times. The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by flash column chromatography to afford the target product as a white solid (192 mg, 95%). MS (m/z) (M~+H): 202, 204.
Computed Properties
Molecular Weight:202.05
XLogP3:2.2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:200.97893
Monoisotopic Mass:200.97893
Topological Polar Surface Area:22.1
Heavy Atom Count:10
Complexity:99.6
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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