Ethylene Glycol → HCID 12813211, compound

HRID 1979822Notes

Reaction equation

HRID 1979822 reaction equation
[CH2:1]([O:8][CH2:9][C:10](=[O:19])[CH2:11][CH2:12][CH:13]1[S:18][CH2:17][CH2:16][CH2:15][S:14]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:20](O)[CH2:21][OH:22].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1C=CC=CC=1>[CH2:1]([O:8][CH2:9][C:10]1([O:22][CH2:21][CH2:20][O:19]1)[CH2:11][CH2:12][CH:13]1[S:18][CH2:17][CH2:16][CH2:15][S:14]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

5

Procedure

Treatment of 1-benzyloxy-4-(1,3-dithian-2-yl)-butan-2-one (89.8 g) in benzene (3.5 l) with distilled ethylene glycol (220 ml) and p-toluenesulfonic acid (11.7 g) at reflux temperature in a Dean-Stark apparatus for 18 hours gives a mixture which is concentrated to 500 ml in vacuo and allowed to stir for one hour. After the addition of sodium carbonate (10 g), the mixture is then partitioned between ether (300 ml) and brine (300 ml). The aqueous phase is extracted with ether (600 ml) and the combined extracts are washed with 0.05% sodium carbonate (1.2 l), filtered through phase-separating paper and dried (sodium sulfate). The solvent is removed in vacuo to give a residue (102.15 g; 99%). A 200 mg portion of the residue is purified on Quantagram PQ1F plates (chloroform) to give 1-benzyloxy-2,2-ethylenedioxy-4-(1,3-dithian-2-yl)-butane (180 mg);

Workup

  1. customgives a mixture which
  2. concentrationis concentrated to 500 ml in vacuo
  3. additionAfter the addition of sodium carbonate (10 g)
  4. customthe mixture is then partitioned between ether (300 ml) and brine (300 ml)
  5. extractionThe aqueous phase is extracted with ether (600 ml)
  6. washthe combined extracts are washed with 0.05% sodium carbonate (1.2 l)
  7. filtrationfiltered
  8. customthrough phase-separating paper
  9. dry with materialdried (sodium sulfate)
  10. customThe solvent is removed in vacuo
  11. customto give a residue (102.15 g; 99%)
  12. customA 200 mg portion of the residue is purified on Quantagram PQ1F plates (chloroform)

Sources & evidence

ORD record
ord-6a9c98f8854540dfabafc3f7a8e96649
Source dataset
uspto-grants-1984_11
Patent number
US04482730

Reaction notes

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