HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → 3-(1-Methyl-1H-tetrazol-5-yl)-5-nitro-benzoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-Methyl-5-nitro-isophthalamic acid ethyl ester | HCID 47099901 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 3-(1-Methyl-1H-tetrazol-5-yl)-5-nitro-benzoic acid ethyl ester | HCID 66733401 | 59.1% |
Reaction Steps
To a 2M solution of N-methyl-5-nitro-isophthalamic acid ethyl ester (10 g) in dichloroethane (200 ml) at −20° C. was added pre-cooled triflic anhydride (10 ml) dropwise. This was stirred for 30 min and then sodium azide (4.6 g) was added. This was allowed to warm to room temperature and stirred overnight. The reaction was neutralised with 5% NaHCO3 (aq) solution and the organic and aqueous layers were separated and the organic layer dried and concentrated in vacuum. Flash chromatography (100:0 to 50:50 gradient cyclohexane:EtOAc) afforded the title compound (6.5 g). Rt=1.52 min (method D).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE045323E1 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-7569141930704fabb34a23bc156c6349 |
| Source note | uspto-grants-2015_01 |