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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490764Generated: October 30, 2026

HCID 63789239, compound → HCID 123498283, compound

https://huagongshe.com/reaction/1490764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 63789239HCID 63789239—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent4,4'-Di-tert-butyl-2,2'-bipyridylHCID 4249187—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventTetrahydrofuranHCID 8028—
ProductHCID 123498283HCID 12349828360%
ProductHCID 178453018HCID 17845301838%

Reaction Conditions

Temperature50 °C

Reaction Steps

Following general procedure F using tert‐butyl (2‐(trifluoromethyl)benzyl)carbamate (68.8 mg, 0.25 mmol), B2pin2 (95 mg, 0.375 mmol), [Ir(COD)OMe]2 (2.5 mg, 0.00375 mmol) and dtbpy (2.0 mg, 0.0075 mmol) in THF (1.25 mL). The reaction was stirred at 50 °C for 20 hours before cooling and the solvents removed. Analysis of crude 1 H NMR using internal standard 1,2‐dimethoxyethane showed 1:1.6 meta:para borylation in 98% yield. As the para isomer could be characterised from the reaction with 1a the product was not isolated.

Provenance & Evidence

DOI10.1002/anie.201708967
Source datasetBorylation dataset from Roche
ORD IDord-1c8694c62b8b46008040a43e875704ba
Source noteBorylation dataset from Roche