HCID 86752880, compound → HCID 22116121, compound

HRID 965300Notes

Reaction equation

HRID 965300 reaction equation
[Cl:1][CH2:2][CH2:3][N:4]1[C:17]2[C:12](=[CH:13][C:14]([F:18])=[CH:15][CH:16]=2)[C:6]2(SCCCS2)[C:5]1=[O:19]>C(O)C.O1CCCC1.[Ni]>[Cl:1][CH2:2][CH2:3][N:4]1[C:17]2[C:12](=[CH:13][C:14]([F:18])=[CH:15][CH:16]=2)[CH2:6][C:5]1=[O:19]

Participants

5

Reactant 1

HCID 86752880HCID 86752880, compound

Product 1

HCID 22116121HCID 22116121, compound

Reagents, catalysts & solvents 3

HCID 935NickelCatalystHCID 702EthanolSolventHCID 8028TetrahydrofuranSolvent

Procedure

1-(2-chloroethyl)-1,3-dihydro-5-fluoro-2-oxo-2H-indole-3-spiro-2'-1,3-dithiane (2.08 g) was dissolved in a mixture of ethanol (30 ml) and tetrahydrofuran (20 ml). Raney nickel was added and the mixture was heated under reflux with vigorous stirring for 3 hours. The cooled solution was filtered, evaporated under reduced pressure and triturated with ether to give 1-(2-Chloroethyl)-5-fluoro-1,3-dihydro-2H-indole-2-one as a white solid.

Workup

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. filtrationThe cooled solution was filtered
  4. customevaporated under reduced pressure
  5. customtriturated with ether

Sources & evidence

ORD record
ord-8bd2901ec4004e68b4c401fc64594873
Source dataset
uspto-grants-1998_06
Patent number
US05773448

Reaction notes

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