Sodium Dithionite → HCID 21404072, compound

HRID 972433Notes

Reaction equation

HRID 972433 reaction equation
COC1C=CC(N=[N:10][C:11]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[CH:14]=[C:13]([S:21]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])(=[O:23])=[O:22])[C:12]=2[OH:42])=CC=1.S(S([O-])=O)([O-])=O.[Na+].[Na+]>C(O)C.O>[NH2:10][C:11]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:14]=[C:13]([S:21]([CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])(=[O:23])=[O:22])[C:12]=1[OH:42]

Participants

5

Procedure

To a suspension of 14 g (0.024 mole) 1-(p-methoxyphenylazo)-3-octadecanesulfonyl-2-naphthol in 500 ml hot ethanol was added a solution of 12 g (0.060 mole) sodium dithionite in 60 ml water. The mixture was stirred and refluxed for one hour, then cooled and filtered to give 11 g of solid, which can be recrystallized from hexane to give a solid, m.p. 84°-88° C.

Workup

  1. temperaturerefluxed for one hour
  2. temperaturecooled
  3. filtrationfiltered

Sources & evidence

ORD record
ord-5547b16c3c2d455d9621734b7252b578
Source dataset
uspto-grants-1977_10
Patent number
US04053312

Reaction notes

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