Chloromethyl Methyl Ether → 3-(Chloromethyl)-2,5-dimethylthiophene

HRID 904460

Reaction equation

HRID 904460 reaction equation
[CH3:1][C:2]1[S:3][C:4]([CH3:7])=[CH:5][CH:6]=1.CO[CH2:10][Cl:11]>C(O)(=O)C>[Cl:11][CH2:10][C:6]1[CH:5]=[C:4]([CH3:7])[S:3][C:2]=1[CH3:1]

Participants

4

Procedure

36.4 G., 0.325 mol. of 2,5-dimethylthiophene, 24.7 g. (0.307 mol) of freshly distilled chloromethyl methyl ether (b.p. 58°-60° C.) and 87.0 g. of glacial acetic acid were combined in a glass pressure bomb and stirred at room temperature for 5 hours. After 0.5 to 1 hr. an exothermic reaction took place. The reaction mixture was cooled externally in an ice bath so that the reaction temperature did not exceed 35° C. The color of the mixture changed from green to blue. The resulting solution was poured into ice water, stirred for ten minutes and extracted four times with benzene. The combined benzene extracts were washed twice with saturated sodium chloride solution, dried and evaporated. The resulting liquid was quickly distilled and the material which boiled at 90°-125° C./18 mm. was collected. A second distillation yielded the pure product, b.p. 109°-115° C./18 mm.

Workup

  1. waitAfter 0.5 to 1 hr
  2. customan exothermic reaction
  3. temperatureThe reaction mixture was cooled externally in an ice bath so that the reaction temperature
  4. customdid not exceed 35° C
  5. stirringstirred for ten minutes
  6. extractionextracted four times with benzene
  7. washThe combined benzene extracts were washed twice with saturated sodium chloride solution
  8. customdried
  9. customevaporated
  10. distillationThe resulting liquid was quickly distilled
  11. customwas collected
  12. distillationA second distillation
  13. customyielded the pure product, b.p. 109°-115° C./18 mm

Sources & evidence

ORD record
ord-9dd96f842b484630aea5c9fdd9337b18
Source dataset
uspto-grants-1980_10
Patent number
US04230872

Linked notes

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