HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1-(2-Methyl-5-thiazolyl)but-1-en-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Methyl-1,3-thiazole-5-carbaldehyde | HCID 13934728 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Methyl-5-thiazolyl)but-1-en-3-one | HCID 54191430 | — |
Reaction Steps
An aqueous solution of 2% sodium hydroxide (3 ml) was added to a solution of 2-methyl-thiazole-5-carboxaldehyde (2.5 g) in acetone (20 ml) and water (10 ml). The mixture was stirred for 24 hours at ambient temperature, diluted with water (150 ml) and extracted with chloroform (2×50 ml). The organic layer was washed with water then dried over anhydrous magnesium sulphate and filtered. Evaporation of the solvent gave 1-(2-methyl-5-thiazolyl)but-1-en-3-one as a low-melting point solid (1.4 g, 43%). Pmr spectrum (CDCl3 ; δ in ppm): 2.30 (3H,s); 2.72 (3H,s); 6.36 (1H,d); 7.56 (1H,d); 7.74 (1H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04604132 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-6a1f60be729348e48e7c4b043cdc20b0 |
| Source note | uspto-grants-1986_08 |