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HCID 22097108, compound → HCID 22097099, compound

HRID 1458856
Notes
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Reaction equation

HRID 1458856 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N+:13]([O-])=O)=[C:6]([NH:8][CH2:9][C:10]([OH:12])=[O:11])[CH:7]=1>C(O)C.[Ni]>[NH2:13][C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][C:6]=1[NH:8][CH2:9][C:10]([OH:12])=[O:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 22097108HCID 22097108, compound

Product 1

HCID 22097099HCID 22097099, compoundYield 93%

Reagents, catalysts & solvents 2

HCID 935NickelCatalystHCID 702EthanolSolvent

Procedure

19.5 g (84.6 mmol) of N-(5-chloro-2-nitrophenyl)glycine were dissolved in 250 ml of ethanol and, after addition of 5 g of Raney nickel, hydrogenated under 1 bar at 45°-50° C. The mixture was then filtered, and the filtrate was evaporated under reduced pressure to yield 15.6 g (93%) of the product.

Workup

  1. customat 45°-50° C
  2. filtrationThe mixture was then filtered
  3. customthe filtrate was evaporated under reduced pressure

Sources & evidence

ORD record
ord-bc4a9ad543d7438a99cf7a56535473cf
Source dataset
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05852017

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes