Acetaldehyde → HCID 178482504, compound

HRID 67727Notes

Reaction equation

HRID 67727 reaction equation
[CH3:1][NH:2][C:3](=[S:6])[NH:4][NH2:5].[CH:7](=O)[CH3:8].N1C=CC=CC=1.[C:16](Cl)(=[O:21])[C:17]([CH3:20])([CH3:19])[CH3:18]>O.C1(C)C=CC=CC=1>[CH3:1][NH:2][C:3]1[S:6][CH:7]([CH3:8])[N:5]([C:16](=[O:21])[C:17]([CH3:20])([CH3:19])[CH3:18])[N:4]=1

Participants

7

Procedure

A 10.5 g. portion of 4-methylthiosemicarbazide was combined with 4.4 g. of acetaldehyde, and 7.9 g. of pyridine and 200 ml. of toluene were added. The mixture was stirred for a short time, and 12.1 g. of pivaloyl chloride was added slowly with agitation while the temperature of the mixture was held at 20°-25°. The mixture was then stirred at ambient temperature for 3 hours, and 50 ml. of water was added. The layers were separated, and the toluene layer was washed with water and was then concentrated under vacuum to obtain 21 g. of oil. The oil was dissolved in 25 ml. of hot nitromethane, filtered and cooled gradually to obtain a solid, which was washed with cold nitromethane and vacuum dried at 50° to obtain 14.8 g. of impure product, which was purified by slurrying it twice with 25 ml. portions of cold nitromethane and vacuum drying to obtain 8.3 g. of product, m.p. 102°-103°.

Workup

  1. customwas held at 20°-25°
  2. stirringThe mixture was then stirred at ambient temperature for 3 hours
  3. customThe layers were separated
  4. washthe toluene layer was washed with water
  5. concentrationwas then concentrated under vacuum
  6. customto obtain 21 g
  7. dissolutionThe oil was dissolved in 25 ml
  8. filtrationof hot nitromethane, filtered
  9. temperaturecooled gradually
  10. customto obtain a solid, which
  11. washwas washed with cold nitromethane and vacuum
  12. customdried at 50°
  13. customto obtain 14.8 g
  14. customof impure product, which was purified
  15. dry with materialportions of cold nitromethane and vacuum drying
  16. customto obtain 8.3 g

Sources & evidence

ORD record
ord-1f5a4e8917884e0aaca0b7e038ef602c
Source dataset
uspto-grants-1982_08
Patent number
US04346225

Reaction notes

Loading…