HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 67004713, 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 67004232 | HCID 67004232 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Product | HCID 67004713 | HCID 67004713 | — |
Reaction Steps
A solution of 1-(4-iodo-5-methyl-1H-pyrazol-1-yl)-2-methylpropan-2-ol (150.0 mg, 0.5355 mmol) in THF (8 mL, 100 mmol) was added 2 M isopropylmagnesium chloride in THF (0.80 mL, 1.6 mmol) at 0° C., and the reaction was allowed to warm to rt over 30 min. 2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.35 mL, 2.1 mmol) was then added, and the mixture was stirred at rt overnight. Sat. NH4Cl was added to quench, and the organic solvent was removed in vacuo. The material was extracted with DCM and water, and 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-3bb1a9bc86dd4c38962110de478cbc25 |
| Source note | uspto-grants-2013_05 |