Potassium Carbonate → HCID 71138918, compound

HRID 539519Notes

Reaction equation

HRID 539519 reaction equation
[CH3:1][O:2][C:3]1[C:4](=[O:9])[NH:5][CH:6]=[CH:7][CH:8]=1.C([O-])([O-])=O.[K+].[K+].[Br:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21]Br)=[CH:19][CH:18]=1>C1COCC1>[Br:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21][N:5]2[CH:6]=[CH:7][CH:8]=[C:3]([O:2][CH3:1])[C:4]2=[O:9])=[CH:19][CH:18]=1

Participants

5

Procedure

To a stirring reaction mixture of 3-methoxypyridine-2-one (2.00 g, 16 mmol) and K2CO3 (4.42 g, 32 mmol) in THF was added 4-bromobenzyl bromide (5.20 g, 20.8 mmol) slowly. Reaction mixture was the heated to reflux and stirring continued overnight. Reaction mixture was then cooled down and separated into organic and aqueous layer by adding CH2Cl2 (120 mL) and water (60 mL). Organic layer was separated and subsequently washed with water (2×60 mL), brine (1×40 mL). Organic layer was dried on Na2SO4 and solvent was evaporated in vacuo. Crude yellowish solid was triturated with hexanes to give pure white solid 145 (3.49 g, 74%) without further purification. 1H NMR (400 MHz, CDCl3) δ 7.25 (m, 2H), 7.04 (m, 2H), 6.78 (dd, J=6.8, 1.2 Hz, 1H), 6.45 (dd, J=7.2, 1.6 Hz, 1H), 5.94 (t, J=7.2 Hz, 1H), 4.95 (s, 2H), 3.64 (s, 3H). 13C NMR (100 MHz, CDCl3) δ 157.71, 149.91, 135.29, 131.49, 129.59, 127.53, 121.57, 111.82, 104.98, 55.54, 51.10. HRMS (EI) calcd for C13H12BrNO2 [M]+ 293.0051. found 293.0051.

Workup

  1. customReaction mixture
  2. temperatureheated
  3. temperatureto reflux
  4. customReaction mixture
  5. temperaturewas then cooled down
  6. customseparated into organic and aqueous layer
  7. additionby adding CH2Cl2 (120 mL) and water (60 mL)
  8. customOrganic layer was separated
  9. washsubsequently washed with water (2×60 mL), brine (1×40 mL)
  10. customOrganic layer was dried on Na2SO4 and solvent
  11. customwas evaporated in vacuo
  12. customCrude yellowish solid was triturated with hexanes

Sources & evidence

ORD record
ord-16a43fb1c1fe4f6697ceb0f214c2ea97
Source dataset
uspto-grants-2014_10
Patent number
US08871728B2

Reaction notes

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