HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Methanol → 2-Chloro-6-methoxypyridine-3-carboxylic acid

HRID 62881
Notes
Print preview

Reaction equation

HRID 62881 reaction equation
[K].[Cl:2][C:3]1[N:11]=[C:10](Cl)[CH:9]=[CH:8][C:4]=1[C:5]([OH:7])=[O:6].[CH3:13][OH:14]>>[Cl:2][C:3]1[N:11]=[C:10]([O:14][CH3:13])[CH:9]=[CH:8][C:4]=1[C:5]([OH:7])=[O:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 887MethanolHCID 8540472,6-Dichloronicotinic acidHCID 5462222Potassium

Product 1

HCID 117692662-Chloro-6-methoxypyridine-3-carboxylic acidYield 52%

Procedure

Potassium botoxide (483 mg, 4.31 mmol) and MeOH (8 mL) were added to 2,6-dichloro-nicotinic acid (207 mg, 1.07 mmol), and the mixture was stirred using microwave at 60° C. for 1 hour. After the termination of the reaction, the reactant was filtered, and 1N HCl was added thereto at 0° C. to adjust the pH to 3. The solid was dried by N2 gas to obtain the title compound (106 mg, 52%).

Workup

  1. customat 60° C.
  2. customfor 1 hour
  3. customAfter the termination of the reaction
  4. filtrationthe reactant was filtered
  5. addition1N HCl was added
  6. customat 0° C.
  7. dry with materialThe solid was dried by N2 gas

Sources & evidence

ORD record
ord-8d8eac4a91ad46bab51f5aec9a772f99
Source dataset
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09447044B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes