Hydrochloric Acid → HCID 67354469, compound

HRID 2272279Notes

Reaction equation

HRID 2272279 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]3[CH:21]=[C:20]([N+:22]([O-])=O)[C:19]([CH:25]4[CH2:27][CH2:26]4)=[CH:18][C:11]=3[C:12]=2[C:13]([O:15][CH2:16][CH3:17])=[O:14])=[CH:4][CH:3]=1.Cl.[H][H]>C(OCC)(=O)C.[Pd]>[NH2:22][C:20]1[C:19]([CH:25]2[CH2:27][CH2:26]2)=[CH:18][C:11]2[C:12]([C:13]([O:15][CH2:16][CH3:17])=[O:14])=[C:8]([C:5]3[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=3)[O:9][C:10]=2[CH:21]=1

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 67354151HCID 67354151, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 67354469HCID 67354469, compoundYield 114.3%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 8857Ethyl AcetateSolvent

Procedure

To a solution of ethyl 2-(4-chlorophenyl)-5-cyclopropyl-6-nitrobenzofuran-3-carboxylate (8 g, 18.2 mmol) in ethyl acetate (450 mL) was added 10% palladium on carbonate (1.83 g), 1N HCl solution (2.5 mL), and stirred with under 0.4 MPa of hydrogen at room temperature for 8 hrs. The reaction mixture was filtered through celite and the filtrate was evaporated under vacuum to give ethyl 6-amino-2-(4-chlorophenyl)-5-cyclopropylbenzofuran-3-carboxylate as a brown solid (7.4 g, 99%).

Workup

  1. filtrationThe reaction mixture was filtered through celite
  2. customthe filtrate was evaporated under vacuum

Sources & evidence

ORD record
ord-34d4684373de42d3817f06efca8402e1
Source dataset
uspto-grants-2015_09
Patent number
US09119868B2

Reaction notes

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