Sulfur dichloride → HCID 54202841, compound

HRID 268475Notes

Reaction equation

HRID 268475 reaction equation
[CH3:1][NH:2][CH:3]=[N:4][C:5]1[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:6]=1[CH3:12].[S:13](Cl)Cl.[CH3:16][NH:17][CH:18]=[N:19][C:20]1[CH:25]=[CH:24][C:23]([CH3:26])=[CH:22][C:21]=1[CH3:27]>CCCCCC.C(N(CC)CC)C.C(Cl)Cl>[CH3:12][C:6]1[CH:7]=[C:8]([Cl:11])[CH:9]=[CH:10][C:5]=1[N:4]=[CH:3][N:2]([S:13][N:17]([CH3:16])[CH:18]=[N:19][C:20]1[CH:25]=[CH:24][C:23]([CH3:26])=[CH:22][C:21]=1[CH3:27])[CH3:1]

Participants

7

Reactant 3

HCID 25353Sulfur dichlorideHCID 178484910HCID 178484910, compoundHCID 178484917HCID 178484917, compound

Product 1

HCID 54202841HCID 54202841, compound

Reagents, catalysts & solvents 3

HCID 6344DichloromethaneSolvent2×HCID 8058HexaneSolventHCID 8471TriethylamineSolvent2×

Conditions

Temperature
-10 °C

Procedure

To a solution of 9.13 g. (0.05 mole) of N-methyl-N'-(2-methyl-4-chlorophenyl)formamidine in 200 ml. of methylene chloride is added 5.05 g. (0.05 mole) of triethylamine. The reaction mixture is cooled to -10° C. and a solution of 5.15 g. (0.05 mole) sulfur dichloride in 5 ml. methylene dichloride is added dropwise keeping the temperature below 0° c. After addition the reaction mixture is allowed to warm to 15° C. About two-thirds of the methylene chloride is removed and 200 ml. of hexane added. The remainder of the methylene chloride is removed and an additional 100 ml. of hexane added. This suspension containing the formamidine sulfenyl chloride is added quickly to a solution of 8.1 g. (0.05 mole) N-methyl-N'-2,4-xylylformamidine and 5.05 g. triethylamine in 300 ml. of hexane with cooling and stirring. The reaction mixture is stirred for 1 hour at room temperature, filtered, and the solvent removed to leave a solid. The crude product is taken up in 200 ml. hexane solution and extracted with 6 g. of citric acid in 100 ml. of water. The hexane solution is dried over MgSO4, filtered, the solvent removed, and the residue recrystallized from Skellysolve B to yield 3.5 g. (18.6%) of product, m.p. 96°-98° C.

Workup

  1. customthe temperature below 0° c
  2. additionAfter addition the reaction mixture
  3. temperatureto warm to 15° C
  4. customAbout two-thirds of the methylene chloride is removed
  5. additionof hexane added
  6. customThe remainder of the methylene chloride is removed
  7. additionof hexane added
  8. additionThis suspension containing the formamidine sulfenyl chloride
  9. additionis added quickly to a solution of 8.1 g
  10. stirringThe reaction mixture is stirred for 1 hour at room temperature
  11. filtrationfiltered
  12. customthe solvent removed
  13. customto leave a solid
  14. extractionhexane solution and extracted with 6 g
  15. dry with materialThe hexane solution is dried over MgSO4
  16. filtrationfiltered
  17. customthe solvent removed
  18. customthe residue recrystallized from Skellysolve B
  19. customto yield 3.5 g

Sources & evidence

ORD record
ord-7759c58a9f7b49a69620dbef0ac57313
Source dataset
uspto-grants-1976_03
Patent number
US03947591

Reaction notes

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