HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490936Generated: October 30, 2026
N-Methylbenzamide → N-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
https://huagongshe.com/reaction/1490936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbenzamide | HCID 11954 | — |
| Reagent | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reagent | 8-([2,2'-bipyridin]-5-yl)quinolin-2(1H)-one | HCID 164681385 | — |
| Catalyst | Bis(1,5-cyclooctadiene)dimethoxydiiridium | HCID 76001521 | — |
| Catalyst | Potassium tert-butoxide | HCID 86639980 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide | HCID 53217108 | 15% |
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-methylbenzamide (27.0 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. After 12 h (judged by GC/MS, conv: 33%), THF was removed under reduced pressure and chromatographic separation with silica gel (15% ethyl acetate in hexane as eluent) gave the metaborylated product 2b (7.8 mg, 15%) as white solid.
Provenance & Evidence
| DOI | 10.1002/anie.201809929 |
|---|
| Source dataset | Borylation dataset from Roche |
|---|
| ORD ID | ord-1c8a8a8e2ca64eeea9380cbf12ba2bc5 |
|---|
| Source note | Borylation dataset from Roche |
|---|