HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(2,4-Dimethyl-5-thiazolyl)but-1-en-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| Reactant | 2,4-Dimethyl-1,3-thiazole-5-carbaldehyde | HCID 2776249 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(2,4-Dimethyl-5-thiazolyl)but-1-en-3-one | HCID 54002730 | 81.8% |
Reaction Steps
A solution of 2,4-dimethylthiazole-5-carboxaldehyde (2.0 g) and 1-triphenylphosphoranylidene-2-propanone (8.2 g) in dimethylsulphoxide (140 ml) was stirred at ambient temperature for 24 hr. The solution was poured into water (400 ml) and extracted with dichloromethane. The dried (Na2SO4) organic extract was evaporated and the residue was purified by column chromatography over silica with ethyl acetate/n-hexane (1:1 v/v) elution to give 1-(2,4-dimethyl-5-thiazolyl)but-1-en-3-one (2.1 g). Pmr spectrum (CDCl3 ; δ in ppm): 2.32 (3H,s); 2.49 (3H,s); 2.67 (3H,s); 6.30 (1H,d); 7.60 (1H,d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04604132 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-1dab19edf9284774b03d9be3c6a4b96e |
| Source note | uspto-grants-1986_08 |