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Water → 3-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

HRID 1416320
Notes
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Reaction equation

HRID 1416320 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:11]#[N:12])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[CH3:13][O:14][CH2:15][C:16]1OC(=O)[S:18][N:17]=1.O>CCCCCCCCCCCC>[CH3:13][O:14][CH2:15][C:16]1[N:12]=[C:11]([S:8]([C:5]2[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][CH:6]=2)(=[O:10])=[O:9])[S:18][N:17]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 87946p-Toluenesulphonyl cyanideHCID 218503335-Methoxymethyl-1,3,4-oxathiazol-2-one

Product 1

HCID 218503733-Methoxymethyl-5-[(4-methylphenyl)-sulfonyl]-1,2,4-thiadiazole

Reagents, catalysts & solvents 1

HCID 8182DodecaneSolvent

Conditions

Temperature
150 °C

Procedure

4-Methylbenzenesulfonyl cyanide (16.26 g) was added to an emulsion of 5-methoxymethyl-1,3,4-oxathiazol-2-one (6.6 g) in dodecane (60 cm3). The reaction mixture was stirred and heated at 150° C. for 18 hours, then cooled. Water was added and the product extracted into ethyl acetate. The combined organic phases were dried (MgSO4) and ethyl acetate was removed by evaporation under reduced pressure. The residue separated into a brown liquid and a clear dodecane layer which was removed and discarded. Chromatography of the brown liquid on silica gel (Sorbsil C30) using 3:7 ethyl acetate:hexane as eluant give a pale orange oil which solidified on standing (6.94 g). M+ =284; 1H NMR: δ 2.40(3H,s); 3.45(3H,s); 4.7(2H,s); 7.4(2H,d); 8.0(2H,d); (mp 43.4-45-4° C.).

Workup

  1. temperaturecooled
  2. extractionthe product extracted into ethyl acetate
  3. dry with materialThe combined organic phases were dried (MgSO4) and ethyl acetate
  4. customwas removed by evaporation under reduced pressure
  5. customThe residue separated into a brown liquid
  6. customa clear dodecane layer which was removed
  7. customhexane as eluant give a pale orange oil which
  8. custom(mp 43.4-45-4° C.)

Sources & evidence

ORD record
ord-1870628798e8491aad2820e66a60204b
Source dataset
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05912243

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes