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Sodium Nitrite → HCID 58136805, compound

HRID 657988
Notes
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Reaction equation

HRID 657988 reaction equation
N[C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:12])([F:11])([F:10])[F:9])[CH:7]=1.N([O-])=[O:18].[Na+]>S(=O)(=O)(O)O.O>[OH:18][C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:12])([F:11])([F:10])[F:9])[CH:7]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 23668193Sodium NitriteHCID 581368521-[3-Amino-5-(pentafluorosulfanyl)phenyl]ethanone

Product 1

HCID 58136805HCID 58136805, compoundYield 54.7%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 1118Sulfuric AcidSolvent

Conditions

Temperature
-5 °C

Procedure

1-[3-Amino-5-(pentafluorosulfanyl)phenyl]ethanone (O4.050; 3.00 g) was dissolved in 35% aqueous sulfuric acid (25 ml) while heating. The solution was cooled to −5° C. and a solution of sodium nitrite (780 mg) in 15 ml of water was added dropwise within 10 min. After 40 min at −5° C., the cooling bath was removed and the mixture was heated to 100° C. for 2 h. After cooling, the mixture was extracted twice with EA. The combined EA phases were washed with saturated sodium hydrogencarbonate solution, dried, filtered and concentrated. The residue was purified using silica gel (80 g cartridge, n-heptane/MtB ether gradient of 0-100% within 40 min). 1.62 g of the title compound were obtained.

Workup

  1. temperaturewhile heating
  2. customthe cooling bath was removed
  3. temperaturethe mixture was heated to 100° C. for 2 h
  4. temperatureAfter cooling
  5. extractionthe mixture was extracted twice with EA
  6. washThe combined EA phases were washed with saturated sodium hydrogencarbonate solution
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe residue was purified
  11. customsilica gel (80 g cartridge, n-heptane/MtB ether gradient of 0-100% within 40 min)

Sources & evidence

ORD record
ord-a8345a17ba2740dabb86fb940532d074
Source dataset
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08076336B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes