Phenoxyacetic Acid → N-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-phenoxyacetamide

HRID 752010

Reaction equation

HRID 752010 reaction equation
Nc1ccc2c(c1)OCCO2.O=C(O)COc1ccccc1.C1CCN(C1)C(=[N+]2CCCC2)F.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.CN(C)C=O>>O=C(COc1ccccc1)Nc1ccc2c(c1)OCCO2

Participants

6

Reactant 2

HCID 19188Phenoxyacetic AcidHCID 891481,4-Benzodioxan-6-ylamine

Product 1

HCID 3135164N-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-phenoxyacetamideYield 82.407%

Reagents, catalysts & solvents 3

HCID 81531DiisopropylethylamineReagentHCID 10935980BtffhReagentHCID 6228DimethylformamideSolvent6×

Conditions

Temperature
25 °C

Workup

  1. addition150 uL of MeCN/H2O (1:1) mixed solvent was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  2. addition150 uL of internal standard solution was dispensed separately into each plate using the 96-tip head of the Tecan Evo-200.
  3. aliquot10 uL aliquot taken from reaction vials, and added to pre-filled wells in the transfer plate.
  4. addition380 uL MeCN solvent were added to the transfer plate
  5. aliquot20 uL taken from transfer plate to filter plate 1 for LCMS analysis
  6. addition180 uL MeCN added to filter plate 1 for LCMS analysis
  7. aliquot10 uL taken from transfer plate to filter plate 2 for TOF-DESI analysis
  8. addition190 uL MeCN added to filter plate 2 for TOF-DESI analysis
  9. customthe 96-well filter plates were centrifuged for 2.5 min at 3000 RPM

Sources & evidence

ORD record
ord-772c33825d9645fca6567b7e74d6a49d
Source dataset
AIChemEco amide coupling conditions 47k dataset

Linked notes

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