Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichloroethanol | HCID 8259 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 57507619 | HCID 57507619 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 69036822 | HCID 69036822 | 73% |
Reaction Steps
To a stirring solution of 3-tert-butyl-1-(3-fluorophenyl)-1H-pyrazole-5-carboxylic acid (0.26 g, 0.60 mmol) and TEA (0.13 ml, 0.90 mmol) in 1,4-dioxane (9 ml) was added DPPA (0.16 ml, 0.75 mmol), After stirring for 30 min at RT, 2,2,2-trichloroethanol (0.58 ml, 6.0 mmol) was added and the reaction was heated at 100° C. for 2 h. The reaction mixture was diluted with brine (10 ml) and extracted with EtOAc (3×20 ml). The combined organic phases were washed with 5% citric acid (10 ml), satd. NaHCO3 (10 ml), dried (MgSO4), filtered and evaporated. The crude product was purified by chromatography to afforded 2,2,2-trichloroethyl 3-tert-butyl-1-(3-fluorophenyl)-1H-pyrazol-5-ylcarbamate (0.180 g, 73% yield) as colorless oil. MS (ESI) m/z: 410(M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188113B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-84d714f6ebcb4b45b9c2040e63b50750 |
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| Source note | uspto-grants-2012_05 |
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