HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095701Generated: October 30, 2026
Tetrahydrofuran → 1-[[(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]methyl]-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
https://huagongshe.com/reaction/2095701
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 10975759 | — |
| Reactant | 1-((S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-4-iodo-5-methyl-1H-pyrazole | HCID 67004621 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Product | 1-[[(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]methyl]-5-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole | HCID 67004538 | — |
Reaction Steps
To a solution of 1-((S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-4-iodo-5-methyl-1H-pyrazole (55.0 mg, 0.171 mmol) in THF (1 mL, 20 mmol) at rt was added 1.3 M of isopropylmagnesium chloride in THF (0.53 mL, 0.68 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 (0.14 mL, 0.85 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 purified via column chromatography, eluting with 5-10% EtOAc/hexanes. The fractions containing the pure product were concentrated in vacuo to afford the title compound as a white solid. MS (ES+): m/z=322.21/323.20/324.20 (50/100/50) [MH+]. HPLC: tR=1.49 min (polar—3 min, UPLC-ACQUITY).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445510B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-505d71aa15fe4cc59be3cb791709559b |
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| Source note | uspto-grants-2013_05 |
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