HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677423Generated: November 1, 2026
2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 59541023, compound
https://huagongshe.com/reaction/1677423
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5017741 | — |
| Reactant | HCID 59540722 | HCID 59540722 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59541023 | HCID 59541023 | 36% |
Reaction Steps
To a −78° C. solution of 1-(5-bromo-2-methoxy-phenyl)-pyrrolidine (270 mg, 1.1 mmol) in THF (17 mL) was added dropwise a solution of t-BuLi (1.3 mL, 1.7 M solution in pentane, 2.2 mmol). The resultant yellow solution was stirred for 30 min, treated with additional t-BuLi (1.3 mL, 1.7 M solution in pentane, 2.2 mmol), stirred for 45 min, and treated dropwise with 2-isopropoxy-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (0.8 mL, 4.4 mmol). The reaction was allowed to slowly warm to room temperature, stirred at room temperature overnight, and partitioned between saturated NH4Cl and EtOAc. The combined organic phases were dried with Na2SO4 and concentrated to give a tan oil. The crude product was purified by flash chromatography using 25 g of silica gel and 0-50% EtOAc in hexanes as eluant to afford 120 mg (35%) of 1-[2-methoxy-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-pyrrolidine as a white solid. M+H 304.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008298B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-ec1c1d3185b2450db95612744d406ef9 |
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| Source note | uspto-grants-2011_08 |
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