HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179537Generated: October 25, 2026
Pyrazole → [3-(1H-Pyrazol-1-yl)phenyl]acetic acid
https://huagongshe.com/reaction/1179537
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Dodecane | HCID 8182 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [3-(1H-Pyrazol-1-yl)phenyl]acetic acid | HCID 21062671 | 65% |
Reaction Steps
Pyrazole (1.2 eq), Cs2CO3 (2.5 eq), CuI (0.5 eq), trans-1,2-cyclohexanediamine (0.6 eq) and dodecane (1 eq), were added to a stirred solution of 3-bromophenylacetic add (1 eq) in dioxane at room temperature under an inert atmosphere. The mixture was irradiated in a microwave reactor (PersonalChemistry Emrys™ Optimiser, 300W, 160° C., 20 min), then added to a 1N aqueous solution of NaOH, and extracted with Et2O. The aqueous phase was acidified to pH=3 with HCl 2N, then extracted with ethyl acetate; this phase was washed with brine, dried over Na2SO4 and the solvent was removed under reduced pressure. The crude material was purified on SPE cartridge (Silica) eluting with a gradient from Cyclohexane/ethyl acetate 8:2, to Cyclohexane/ethyl acetate 1:1, affording the title compound in 65% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279481B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-bc919c8883a84953abab0f1dc955e1b3 |
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| Source note | uspto-grants-2007_10 |
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