Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Semicarbazide | HCID 5196 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-(Benzyloxy)-2,2-dimethylpropanoic acid | HCID 13478288 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 136641697 | HCID 136641697 | 48% |
Reaction Steps
3-(Benzyloxy)-2,2-dimethylpropanoic acid (1.00 g, 4.80 mmol) was dissolved in DCM (10 mL) at RT. Oxalyl chloride (0.70 mL, 8.00 mmol) and DMF (0.10 mL, 1.29 mmol) were added sequentially and the reaction mixture was stirred at RT for 2 h. In a separate flask, semicarbazide hydrochloride (0.8 g, 7.24 mmol) and NaOH (0.80 g, 20.0 mmol) were dissolved in a solution of dioxane (2.0 mL) and water (10.0 mL). The solution of the acid chloride was added in one portion to the solution of the semicarbazide and the reaction mixture was stirred at RT for 12 h. 2 M NaOH (aq.) (28.0 mL, 56.0 mmol) was then added and the reaction mixture was stirred at 100° C. for 2 h, allowed to cool to RT, and neutralized by the addition of ¾ sat. NH4Cl (aq.) (75 mL). The resultant homogenous solution was sonicated for 12 h and the resultant precipitated solids were collected by filtration and dried in vacuo to afford 3-(1-(benzyloxy)-2-methylpropan-2-yl)-1H-1,2,4-triazol-5(4H)-one (0.57 g, 48.0%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 11.22 (s, 1H), 11.09 (s, 1H), 7.34-7.23 (m, 5H), 4.44 (s, 2H), 3.39 (s, 2H), 1.16 (s, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193719B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-b8b710ae593e462e8327a0b6f622729f |
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| Source note | uspto-grants-2015_11 |
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