4-Chlorobenzaldehyde → HCID 54455287, compound

HRID 1033535Notes

Reaction equation

HRID 1033535 reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([S:17]([NH2:20])(=[O:19])=[O:18])=[CH:13][CH:12]=1>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[N:20][S:17]([C:14]2[CH:13]=[CH:12][C:11]([Cl:10])=[CH:16][CH:15]=2)(=[O:19])=[O:18])=[CH:4][CH:3]=1

Participants

4

Procedure

A stirred solution consisting of 7.03 g (5.0 mmol) of 4-chlorobenzaldehyde, 9.58 g (5.0 mmol) of 4-chlorobenzenesulfonamide, 8 g of 4A molecular sieves and 0.1 g of Amberlite IR-120 in 90 mL of toluene was heated to reflux. The reaction vessel was fitted with a Dean Stark trap which was filled with 4A molecular sieves. The mixture was heated for 4 hours, at which point TLC analysis showed conversion to sulfonimine. The mixture was allowed to cool to room temperature and was filtered. Concentration of the filtrate and subsequent recrystallization of the crude product from CHCl3 - hexane gave 7.84 g (50%) of sulfonimine as a white crystalline material: IR 3090, 1598, 1582, 1553, 1321, 1084 cm-1 ; 1H NMR (CDCl3, TMS, 60 MHz) & 9.02 (s, 1), 7.73 (A2B2, 4, Δν=24 Hz, JAB =8 Hz), 7.67 (A2 B2, 4,Δν=23 Hz, JAB =9 Hz); m p. 128.0 ° C.

Workup

  1. temperaturewas heated to reflux
  2. customThe reaction vessel was fitted with a Dean Stark trap which
  3. temperatureThe mixture was heated for 4 hours, at which point TLC analysis
  4. filtrationwas filtered
  5. customConcentration of the filtrate and subsequent recrystallization of the crude product from CHCl3 - hexane
  6. customgave 7.84 g (50%) of sulfonimine as a white crystalline material
  7. custom128.0 ° C.

Sources & evidence

ORD record
ord-201219c256cc4ec2b2ea79d6089d4839
Source dataset
uspto-grants-1994_05
Patent number
US05310925

Reaction notes

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