Ethanol → HCID 178464376, compound

HRID 893887Notes

Reaction equation

HRID 893887 reaction equation
C([S:3]([CH2:6][CH2:7][N:8]([CH2:16][CH3:17])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[CH:10]=1)(=[O:5])=[O:4])=C.[S:18](=[O:21])(O)[O-:19].[Na+:22].[CH2:23](O)[CH3:24].[OH2:26]>>[Na:22][CH:6]([S:3]([OH:4])(=[O:5])=[O:26])[CH2:7][N:8]([CH2:16][CH3:17])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[C:10]=1[CH2:23][CH:24]=[S:18](=[O:21])=[O:19]

Participants

5

Procedure

N-(2-vinylsulfonylethyl-N-ethyl-m-toluidine (25.3 g, 0.1 m) in water solution (100 ml) is stirred with sodium bisulfite (11.0 g, 0.1 m). The reaction is heated to reflux and held for 15 min. The clear solution is drowned into ethanol (200 ml) and allowed to cool. The white solid is collected by filtration, air dried and melts at 237°-240° C.

Workup

  1. temperatureThe reaction is heated
  2. temperatureto reflux
  3. temperatureto cool
  4. filtrationThe white solid is collected by filtration, air
  5. customdried

Sources & evidence

ORD record
ord-05cb9f0e2a4748858dce4cd0ed5ecdb5
Source dataset
uspto-grants-1981_08
Patent number
US04282144

Reaction notes

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