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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490969Generated: October 30, 2026

HCID 792123, compound → HCID 178457666, compound

https://huagongshe.com/reaction/1490969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 792123HCID 792123—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent8-([2,2'-bipyridin]-5-yl)quinolin-2(1H)-oneHCID 164681385—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
CatalystPotassium tert-butoxideHCID 86639980—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178457666HCID 17845766696%

Reaction Conditions

Temperature80 °C

Reaction Steps

In an argon filled glove box, a 5.0 mL wheaton microreactor was charged with [Ir(cod)(OMe)]2 (1.98 mg, 1.5 mol%), L1 ligand (2.1 mg, 3.5 mol%), B2pin2 (50.8 mg, 1.0 equiv.), KOtBu (1.0 mg, 4.5 mol%) and dry THF (1.0 mL). The reaction mixture was stirred for 2 minutes at room temperature. To this mixture, N,N-diisopropylthiophene-2-carboxamide (42.3 mg, 0.2 mmol) was added. The microreactor was capped with a teflon pressure cap and placed into pre-heated aluminum block at 80 oC. The reaction mixture was stirred for 12 h. After completion (judged by GC/MS), THF was removed under reduced pressure and chromatographic separation with silica gel (10% ethyl acetate in hexane as eluent) gave the meta-borylated product 8b (64.8 mg, 96%) as white solid.

Provenance & Evidence

DOI10.1002/anie.201809929
Source datasetBorylation dataset from Roche
ORD IDord-f9f11335416b4824a6229c3913644d4a
Source noteBorylation dataset from Roche