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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490982Generated: October 30, 2026

HCID 14267491, compound → tert-Butyl methyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate

https://huagongshe.com/reaction/1490982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14267491HCID 14267491—
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—
Producttert-Butyl methyl[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamateHCID 6714827591%

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 (2.19 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, tert-butyl methyl(phenyl)carbamate (41.4 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 (8% ethyl acetate in hexane as eluent) gave the meta-borylated product 8o (60.6 mg, 91%) as liquid.

Provenance & Evidence

DOI10.1002/anie.201809929
Source datasetBorylation dataset from Roche
ORD IDord-9e1caa3eb5d24482b141e29b9890aee5
Source noteBorylation dataset from Roche