2-(Cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → Biphenyl

HRID 608299Notes

Reaction equation

HRID 608299 reaction equation
CC1(C)OB(C2=CCCCC2)OC1(C)C.CN1C(=O)C[C@@](C)(c2sccc2Cl)N/C1=N/C(=O)OC(C)(C)C.O=P(O)(O)O.[K]>CC(C)c1cc(C(C)C)c(-c2ccccc2[PH](C2CCCCC2)(C2CCCCC2)[Pd]2([O]S(C)(=O)=O)[NH]c3ccccc3-c3cccc[c]32)c(C(C)C)c1.CS(C)=O.O>CN1C(=O)C[C@@](C)(c2sccc2C2=CCCCC2)N/C1=N/C(=O)OC(C)(C)C

Participants

9

Reactant 2

HCID 109326752-(Cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 178481525HCID 178481525, compound

Product 3

HCID 7095BiphenylHCID 178481517HCID 178481517, compoundHCID 178481525HCID 178481525, compound

Reagents, catalysts & solvents 4

HCID 178439024HCID 178439024, compoundCatalystHCID 679Dimethyl SulfoxideSolvent3×HCID 962WaterSolvent2×HCID 16218557Phosphoric acid (potassium)Other

Workup

  1. additionAfter 22 hours the crude reactions were diluted with 3 x 1 uL 0.5 M AcOH in DMSO (containing PhPh as an internal standard). The reactions were mixed after each dispense operation.
  2. aliquotMosquito(R) was used to transfer 1 uL of each quenched reaction from the 1,536-well reaction plate to 384-well analytical plates containing 60 uL DMSO for analysis.

Sources & evidence

ORD record
ord-1f25fda662e14a08ba5b62b62dd7b32c
Source dataset
Cernak miniaturized Suzuki Cross-Coupling 12x10 Informer Library
Original link
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Reaction notes

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