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Potassium Carbonate → (S)-3-(2-bromopyridine-3-yloxy)-2-methyl-1-propanol

HRID 496812
Notes
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Reaction equation

HRID 496812 reaction equation
[Br:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:16][C@@H:17]([CH3:20])[CH2:18][OH:19]>CC(CC)=O>[Br:1][C:2]1[C:7]([O:8][CH2:16][C@@H:17]([CH3:20])[CH2:18][OH:19])=[CH:6][CH:5]=[CH:4][N:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 230702-Bromo-3-pyridinolHCID 10986449(S)-(+)-3-Bromo-2-methyl-1-propanol

Product 1

HCID 86595488(S)-3-(2-bromopyridine-3-yloxy)-2-methyl-1-propanolYield 80%

Reagents, catalysts & solvents 1

HCID 6569Methyl Ethyl KetoneSolvent

Conditions

Temperature
100 °C

Procedure

2-bromo-3-pyridinol (230 mg) and potassium carbonate (216 mg) was dissolved in methylethylketone (10 ml) and reacted for 30 minutes. Then, (S)-3-bromo-2-methyl-1-propanol (0.21 ml) was added to the solution and refluxed for 3 hours at 100° C. Potassium carbonate was filtered out and separated by flash chromatography under a silica gel phase (ethyl acetate:normal hexane=1:1). As a result, (S)-3-(2-bromopyridine-3-yloxy)-2-methyl-1-propanol (260 mg, yield: 80%) was obtained.

Workup

  1. customreacted for 30 minutes
  2. filtrationPotassium carbonate was filtered out
  3. customseparated by flash chromatography under a silica gel phase (ethyl acetate:normal hexane=1:1)

Sources & evidence

ORD record
ord-1d4369e11c0b4f37ad8dccad06fee476
Source dataset
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06946558B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes