4-tert-butyl-N-methylbenzamide → HCID 178485327, compound

HRID 1491063Notes

Reaction equation

HRID 1491063 reaction equation
CNC(=O)c1ccc(C(C)(C)C)cc1>C1=CCCC=CCC1.C1=CCCC=CCC1.C1CCOC1.CC1(C)OB(B2OC(C)(C)C(C)(C)O2)OC1(C)C.C[OH2+].C[OH2+].Cc1[nH]c2c(NC(=O)c3ccc(-c4ccccn4)nc3)cccc2c1C.[Ir].[Ir]>CNC(=O)c1ccc(C(C)(C)C)cc1B1OC(C)(C)C(C)(C)O1

Participants

6

Reactant 1

HCID 1812574-tert-butyl-N-methylbenzamide

Product 1

HCID 178485327HCID 178485327, compoundYield 41%

Reagents, catalysts & solvents 4

HCID 2733548Bis(pinacolato)diboraneReagentHCID 178433626HCID 178433626, compoundReagentHCID 76001521Bis(1,5-cyclooctadiene)dimethoxydiiridiumCatalystHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
60 °C

Procedure

Isolated by chromatography using deactivated silica gel and ethyl acetate and petroleum ether (10:1 to 1:1) as the eluent.

Sources & evidence

ORD record
ord-8a014e76d53e4bd5920e1da16799d6de
Source dataset
Borylation dataset from Roche

Reaction notes

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