Ethyl orthoformate → methyl 2-methylthio-5-(1H-tetrazol-1-yl)benzoate
Reaction equation
[CH3:1][S:2][C:3]1[CH:12]=[CH:11][C:10]([NH2:13])=[CH:9][C:4]=1[C:5]([O:7][CH3:8])=[O:6].[CH:14](OCC)(OCC)OCC.[N-:24]=[N+:25]=[N-:26].[Na+]>C(O)(=O)C.O>[CH3:1][S:2][C:3]1[CH:12]=[CH:11][C:10]([N:13]2[CH:14]=[N:26][N:25]=[N:24]2)=[CH:9][C:4]=1[C:5]([O:7][CH3:8])=[O:6]Participants
6
Conditions
- Temperature
- 70 °C
Procedure
Combine methyl 2-methylthio-5-aminobenzoate (2.18 g, 11.1 mmol) and triethyl orthoformate (7.4 mL, 44.3 mmol) in glacial acetic acid (20 mL). After the formation of a yellow solid, add glacial acetic acid (40 mL). After 50 minutes, add sodium azide (2.9 g, 44.3 mmol). Heat to 70° C. After 2 hours, cool the reaction mixture to ambient temperature and stir. After 56 hours, cool in an ice bath and dilute with water (400 mL) to give a solid. After 1 hour, collect the solid by filtration, rinse with water, and dry to give methyl 2-methylthio-5-(1H-tetrazol-1-yl)benzoate: Rf=0.90 (silica gel, 10% methanol/ethyl acetate).
Workup
- waitAfter 2 hours
- temperaturecool the reaction mixture to ambient temperature
- waitAfter 56 hours
- temperaturecool in an ice bath
- customto give a solid
- waitAfter 1 hour
- customcollect the solid
- filtrationby filtration
- washrinse with water
- customdry
Sources & evidence
- ORD record
- ord-5bade1db7246485caa28f2d476b5ed85
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06211199B1
Reaction notes
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