Sulfuric Acid → HCID 57435159, compound

HRID 1434817Notes

Reaction equation

HRID 1434817 reaction equation
[N+:1]([CH:4]([CH3:15])[CH:5]([OH:14])[CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)([O-:3])=[O:2].S(=O)(=O)(O)O.[C:21](OC(=O)C)(=[O:23])[CH3:22]>C(Cl)Cl>[N+:1]([CH:4]([CH3:15])[CH:5]([O:14][C:21](=[O:23])[CH3:22])[CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)([O-:3])=[O:2]

Participants

5

Procedure

Crude 4-Nitro-1-phenyl-pentan-3-ol (179) from above was dissolved in CH2Cl2 (60 mL) and cooled in an ice bath under nitrogen. Concentrated sulfuric acid (0.76 mL, 14.2 mmol) then acetic anhydride (13.83 mL, 146.2 mmol) were added slowly, and the reaction was allowed to warm to room temperature, and was stirred until judged complete by HPLC (3 h, 40 min). (Note: The reaction turned black soon after the addition of the acetic anhydride.) The reaction was quenched by pouring slowly into water, then the organic layer was removed, washed with aq. NaHCO3, dried, filtered, and concentrated. The crude product was purified by purified by silica gel chromatography (Combiflash column, 95:5 Hexanes:EtOAc) to achieve pure 180 (21.4447 g, 65.5%, 2 steps). HPLC: 10.45 min.

Workup

  1. temperaturecooled in an ice bath under nitrogen
  2. customuntil judged complete by HPLC (3 h, 40 min)
  3. custom) The reaction was quenched
  4. additionby pouring slowly into water
  5. customthe organic layer was removed
  6. washwashed with aq. NaHCO3
  7. customdried
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude product was purified
  11. customby purified by silica gel chromatography (Combiflash column, 95:5 Hexanes:EtOAc)
  12. custom10.45 min.

Sources & evidence

ORD record
ord-8e646ef1b271431da740552becd35c74
Source dataset
uspto-grants-2009_11
Patent number
US07615572B2

Reaction notes

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