2-Methoxyethanol → CID 101686797

HRID 1164240Notes

Reaction equation

HRID 1164240 reaction equation
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O-:14])(=[O:13])=[O:12].[Na+:15].[CH3:16][O:17][CH2:18][CH2:19][OH:20].[OH-].[Na+]>[O-2].[O-2].[Mn+4].O>[CH3:16][O:17][CH2:18][CH2:19][O:20][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]([O-:14])(=[O:13])=[O:12].[Na+:15]

Participants

6

Reactant 3

HCID 80192-MethoxyethanolHCID 14798Sodium HydroxideHCID 70350Benzenesulfonic acid, 2-chloro-5-nitro-, sodium salt (1:1)

Product 1

HCID 101686797CID 101686797

Reagents, catalysts & solvents 2

HCID 178418406HCID 178418406, compoundCatalystHCID 962WaterSolvent

Conditions

Temperature
75 °C

Procedure

5.2 g of sodium 2-chloro-5-nitrobenzenesulfonate, 0.6 g of manganese dioxide, 15 ml of methyl cellosolve, 1 ml of water, and 0.95 g of sodium hydroxide were mixed and stirred at 75° C. for 40 minutes. After cooling, insolubles were filtered, and the filtrate was poured into 100 ml of isopropyl alcohol. Crystals thus formed were collected by filtration to obtain 4.8 g of sodium 2-(2-methoxyethoxy)-5-nitrobenzenesulfonate. m.p. 238° to 239° C.

Workup

  1. temperatureAfter cooling
  2. filtrationinsolubles were filtered
  3. additionthe filtrate was poured into 100 ml of isopropyl alcohol
  4. customCrystals thus formed
  5. filtrationwere collected by filtration

Sources & evidence

ORD record
ord-025e6513147d4920997354ed900e70d1
Source dataset
uspto-grants-1983_01
Patent number
US04368251

Reaction notes

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