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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095712Generated: November 2, 2026

Tetrahydrofuran → HCID 178431102, compound

https://huagongshe.com/reaction/2095712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 10975759—
ReactantHCID 178418918HCID 178418918—
ReactantHCID 178455357HCID 178455357—
ProductHCID 178431102HCID 178431102—

Reaction Steps

To a solution of [1-(trans-4-{[tert-butyl(dimethyl)silyl]oxy}cyclohexyl)-4-iodo-1H-pyrazol-5-yl]methanol (40.0 mg, 0.0916 mmol) in THF (2 mL, 20 mmol) at rt was added 1.3 M of isopropylmagnesium chloride in THF (0.28 mL, 0.37 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 (0.075 mL, 0.46 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. MS (ES+): m/z=437.29 (100) [MH+]. HPLC: tR=1.94 min (polar—3 min, UPLC-ACQUITY).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445510B2
Source datasetuspto-grants-2013_05
ORD IDord-4f1946cd95414d8ca9671c9f48c305a0
Source noteuspto-grants-2013_05