Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19790067 | HCID 19790067 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19790260 | HCID 19790260 | 68% |
Reaction Steps
To an aqueous solution (27 ml) of sodium hydroxide (2.1 g) were added ethyl 2-(5-tritylamino-2H-tetrazol-2-yl)acetate (14.2 g), methanol (50 ml) and tetrahydrofuran (100 ml), and the mixture was stirred at 40° C. for 2 hours. After the organic solvent was removed by evaporation, to the residue were added water (50 ml) and ethyl acetate (50 ml), followed by separating out the aqueous layer. Thereto was added ethyl acetate (100 ml) and then adjusted to pH 1.5 with 10% hydrochloric acid. The aqueous solution was washed with an aqueous sodium chloride (50 ml) and dried over magnesium sulfate. Removal of the solvent gave a residue, which was pulverized with diisopropyl ether to obtain 2-(5-tritylamino-2H-tetrazol-2-yl)acetic acid (9.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04423213 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-538923f840754c899c9dadb28be35a49 |
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| Source note | uspto-grants-1983_12 |
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