HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 178437968, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 10975759 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Reactant | HCID 178437969 | HCID 178437969 | — |
| Product | HCID 178437968 | HCID 178437968 | — |
Reaction Steps
To a solution of trans-4-(3-ethyl-4-iodo-1H-pyrazol-1-yl)cyclohexanol (150.0 mg, 0.4685 mmol) in THF (10 mL, 100 mmol) at rt was added 2 M isopropylmagnesium chloride in THF (0.70 mL, 1.4 mmol), and the mixture was stirred for 1 h. The reaction was quenched with 2-methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.31 mL, 1.9 mmol), and allowed to stir at rt for 1 h. Sat. NH4Cl was added, and the organic solvent was removed in vacuo. The material was extracted with DCM and water. The organic layer was concentrated in vacuo to afford the title compound as a white solid. The material was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445510B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-51d1a75a62fc49538ad0c4474b160b48 |
| Source note | uspto-grants-2013_05 |