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Water → 4-Cyano-5-(2-nitro-5-phenoxy-phenyl)-pentanoic acid

HRID 252462
Notes
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Reaction equation

HRID 252462 reaction equation
[N+:1]([C:4]1[CH:17]=[CH:16][C:15]([O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:14][C:5]=1[CH2:6][CH:7]([CH2:10][CH2:11][CH:12]=C)[C:8]#[N:9])([O-:3])=[O:2].I([O-])(=O)(=O)=[O:26].[Na+].ClCCl.[OH2:34]>C(#N)C.C(Cl)(Cl)(Cl)Cl.[Ru](Cl)(Cl)Cl>[C:8]([CH:7]([CH2:6][C:5]1[CH:14]=[C:15]([O:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:16]=[CH:17][C:4]=1[N+:1]([O-:3])=[O:2])[CH2:10][CH2:11][C:12]([OH:26])=[O:34])#[N:9]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 962WaterHCID 6344DichloromethaneHCID 23667635Sodium periodateHCID 574757192-(2-Nitro-5-phenoxy-benzyl)-hex-5-enenitrile

Product 1

HCID 574757204-Cyano-5-(2-nitro-5-phenoxy-phenyl)-pentanoic acid

Reagents, catalysts & solvents 3

HCID 61850
Ruthenium trichloride
Catalyst
HCID 5943Carbon TetrachlorideSolvent
HCID 6342AcetonitrileSolvent

Procedure

2-(2-nitro-5-phenoxy-benzyl)-hex-5-enenitrile (1.07 g, 3.31 mmol) was dissolved in a mixture of acetonitrile (10 mL) and carbon tetrachloride (10 mL). In a separate vial sodium periodate (2.84 g, 13.28 mmol) was dissolved in water (15 mL), and this solution was added to the reaction mixture followed by ruthenium trichloride (0.021 g, 0.100 mmol). The reaction mixture was stirred vigorously for 16 h, and the next morning the reaction mixture was added to a separatory funnel with dichloromethane. The organic layer was washed 3 times with 1N HCl and one time with saturated brine solution. The organic layer was dried with sodium sulfate, filtered and the solvent was removed under reduced pressure to yield a residue.

Workup

  1. additionthis solution was added to the reaction mixture
  2. washThe organic layer was washed 3 times with 1N HCl and one time with saturated brine solution
  3. dry with materialThe organic layer was dried with sodium sulfate
  4. filtrationfiltered
  5. customthe solvent was removed under reduced pressure
  6. customto yield a residue

Sources & evidence

ORD record
ord-b12678e114b6425e8e900554c42756f3
Source dataset
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07868022B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes