HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601456Generated: October 25, 2026
2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 4,4,5,5-Tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolane
https://huagongshe.com/reaction/601456
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 5017741 | — |
| Reactant | 1-Iodo-4-octylbenzene | HCID 11594836 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,4,5,5-Tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolane | HCID 58823386 | — |
Reaction Steps
n-BuLi (16.6 mL, 1.6 M in hexanes) was added over 10 minutes to a solution of 1-iodo-4-octylbenzene from Part A (6.9 g, 21.8 mmol) in dry THF (100 mL) at −78° C. under a nitrogen atmosphere. The mixture was stirred for another 10 minutes at −78° C. 2-Isopropoxy-4,4,5,5-tetramethyl[1,3,2]dioxaborolane (6.21 mL, 30.4 mmol) was subsequently added dropwise to the mixture and stirring was continued at room temperature overnight. The reaction was then quenched with distilled water, and THF was removed under vacuum. The product was then extracted into diethyl ether and the organic layer was washed with brine, dried over MgSO4, filtered and evaporated in vacuo to give 6.38 g of 4,4,5,5-tetramethyl-2-(4-octylphenyl)-1,3,2-dioxaborolane as a colorless oil. The product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902363B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-e2477bd9e1ec49968840cad319376436 |
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| Source note | uspto-grants-2011_03 |
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