Water → HCID 86675539, compound

HRID 1624216Notes

Reaction equation

HRID 1624216 reaction equation
[SH:1][CH2:2][C:3]1[N:4]=[C:5]([CH3:13])[S:6][C:7]=1[C:8](OCC)=[O:9].O>O1CCCC1>[SH:1][CH2:2][C:3]1[N:4]=[C:5]([CH3:13])[S:6][C:7]=1[CH:8]=[O:9]

Participants

4

Procedure

10 mmol of ethyl 4-(mercaptomethyl)-2-methyl-1,3-thiazole-5-carboxylate was dissolved in 100 ml of dried tetrahydrofuran, then 42 ml of 0.5M SDBBA solution was gradually added with keeping the temperature at −30 to −20° C. After the adding, the reaction was carried out for 4 hours at −20° C. Then 20 ml of water was added into the reaction system to stop the reaction and then an organic layer was separated. To the remaining water phase, sodium hydrogen carbonate was added until the pH of the water phase reached a value of 8 to 9. The product was extracted and separated into an organic layer using ethyl acetate. This organic layer and the previous organic layer were mixed together and dried under sodium sulfate. The solvent was evaporated out and then the product was purified using a column separation with solvents of ethylacetate and hexane, obtaining 4-(mercaptomethyl)-2-methyl-1,3-thiazole-5-carbaldehyde.

Workup

  1. addition42 ml of 0.5M SDBBA solution was gradually added
  2. customat −30 to −20° C
  3. customthe reaction
  4. customan organic layer was separated
  5. additionTo the remaining water phase, sodium hydrogen carbonate was added until the pH of the water phase
  6. extractionThe product was extracted
  7. customseparated into an organic layer
  8. additionThis organic layer and the previous organic layer were mixed together
  9. customdried under sodium sulfate
  10. customThe solvent was evaporated out
  11. customthe product was purified
  12. customa column separation with solvents of ethylacetate and hexane

Sources & evidence

ORD record
ord-dec555f04f284ef997b39ea5220f6252
Source dataset
uspto-grants-2014_07
Patent number
US08779086B2

Reaction notes

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