Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Hydrazinoethanol | HCID 8017 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Benzyloxyacetaldehyde diethyl acetal | HCID 4321487 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67486330 | HCID 67486330 | 17.6% |
Reaction Steps
POCl3 (12.9 ml, 141.2 mmol) was added to DMF (10.9 ml, 141.2 mmol) at 0° C. The reaction was immediately warmed to ambient temperature and was stirred for 30 minutes. ((2,2-Diethoxyethoxy)methyl)benzene (10.6 g, 47.1 mmol) was added as a solution in 80 mL of chloroform. The solution was stirred at 75° C. for 3.5 hours. The solution was cooled, poured over ice water, and neutralized with Na2CO3. The residue was extracted with chloroform and the organic layer was dried with Na2SO4 and concentrated. The residue was re-dissolved in MeOH (450 mL). NaOMe (25% in MeOH, 58 ml, 253 mmol) was added followed by 2-hydrazinylethanol (10.6 g, 139 mmol). The reaction was stirred overnight at ambient temperature. The material was concentrated in vacuo followed by dilution with saturated NH4Cl solution. The material was extracted with EtOAc, dried (MgSO4), and concentrated. Flash chromatography of the crude material gave 2-(4-(benzyloxy)-1H-pyrazol-1-yl)ethanol (1.81 g, 13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362037B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-5dc3d39f83ed481683eb3a709afa60ac |
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| Source note | uspto-grants-2013_01 |
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