Methanol → 2-(4-(2H-1,2,3-triazol-2-yl)phenyl)-2-methoxyacetic acid
Reaction equation
[N:1]1[N:2]([C:6]2[CH:13]=[CH:12][C:9]([CH:10]=[O:11])=[CH:8][CH:7]=2)[N:3]=[CH:4][CH:5]=1.[CH:14](Br)(Br)Br.[OH-:18].[K+].[CH3:20][OH:21]>>[N:1]1[N:2]([C:6]2[CH:7]=[CH:8][C:9]([CH:10]([O:11][CH3:14])[C:20]([OH:21])=[O:18])=[CH:12][CH:13]=2)[N:3]=[CH:4][CH:5]=1Participants
Procedure
To a solution of 4-(2H-1,2,3-triazol-2-yl)benzaldehyde (1.0 g, 5.77 mmol) in anhydr MeOH (15 mL) at 0° C. (bath temperature) was added bromoform (1.82 g, 7.21 mmol) with stirring. Solid KOH (1.62 g, 28.9 mmol) was added in aliquots over a period of 10 min. The mixture was stirred for 1 hour and the cold bath was removed. After stirring for 30 min, the reaction was allowed to warm slowly to room temperature overnight then concentrated to dryness. After dissolving in a minimum amount of H2O, the residue was acidified to pH 1 with 6 M HCl. The aqueous mixture was extracted with EtOAc several times with the addition of brine to the aqueous layer during extraction. The combined organics were washed with brine, dried over Na2SO4 and concentrated in vacuo to give 2-(4-(2H-1,2,3-triazol-2-yl)phenyl)-2-methoxyacetic acid as an oil (1.19 g, 88% yield). The product was used without further purification.
Workup
- stirringThe mixture was stirred for 1 hour
- customthe cold bath was removed
- stirringAfter stirring for 30 min
- concentrationthen concentrated to dryness
- dissolutionAfter dissolving in a minimum amount of H2O
- extractionThe aqueous mixture was extracted with EtOAc several times with the addition of brine to the aqueous layer during extraction
- washThe combined organics were washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-6d8d51a266cc4683a41dfa8d21e5c4de
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08343970B2
Reaction notes
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