HCID 86743030, compound → HCID 86743029, compound

HRID 1761982Notes

Reaction equation

HRID 1761982 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([S:10]([C:13]([OH:37])([S:25]([C:28]2[CH:33]=[CH:32][C:31]([N+:34]([O-])=O)=[CH:30][CH:29]=2)(=[O:27])=[O:26])[CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][O:21][CH2:22][CH2:23][OH:24])(=[O:12])=[O:11])=[CH:6][CH:5]=1)([O-])=O>C(OCC)(=O)C.[Pd]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([S:10]([C:13]([OH:37])([S:25]([C:28]2[CH:29]=[CH:30][C:31]([NH2:34])=[CH:32][CH:33]=2)(=[O:27])=[O:26])[CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][O:21][CH2:22][CH2:23][OH:24])(=[O:11])=[O:12])=[CH:8][CH:9]=1

Participants

4

Procedure

Bis-(4-nitrobenzenesulfonyl)-tetraethylene glycol (10 g, from Part A) was dissolved in distilled ethyl acetate (200 ml) and hydrogenated over palladium on carbon (10%, 0.5 g) at 40 p.s.i. in a Parr hydrogenation apparatus. The solution was filtered and evaporated under reduced pressure to give bis-(4-aminobenzenesulfonyl)-tetraethylene glycol in quantitative yield as a thick, yellow oil which was homogeneous by TLC.

Workup

  1. filtrationThe solution was filtered
  2. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-cda961a82a9e40f992659be7d154e426
Source dataset
uspto-grants-1989_05
Patent number
US04829099

Reaction notes

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