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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479122Generated: November 2, 2026

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 131736572, compound

https://huagongshe.com/reaction/1479122

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
ReactantHCID 117601456HCID 117601456—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 131736572HCID 13173657265.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Into a solution of 4-(9,9-dimethyl-9H-fluoren-2-yl)dibenzo[b,d]thiophene (10.637 g, 28.3 mmol) in THF (200 ml), a solution of sec-butyllithium 1.4 M (27.2 ml, 38.1 mmol) in cyclohexane at −78° C. was added slowly. The resulting mixture was stirred at −78° C. for 2 hours before quenching with 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (8.65 ml, 42.4 mmol) added at one portion. The mixture was gradually warmed to room temperature, stirred overnight, and then quenched with methanol. The solvent was evaporated. The residue was purified by column chromatography on silica gel with a heptane/DCM (4/1 to 1/1) eluent and then precipitation in MeOH to yield 2-(6-(9,9-dimethyl-9H-fluoren-2-yl)dibenzo[b,d]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (9.3 g, 65.5% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09406892B2
Source datasetuspto-grants-2016_08
ORD IDord-8b642c933dd248e1879a232627af4c64
Source noteuspto-grants-2016_08