HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → HCID 178499520, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 4-(Dimethylamino)-1,1-dimethoxybut-3-en-2-one | HCID 2782145 | — |
| Reactant | Potassium methoxide | HCID 23664618 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178499520 | HCID 178499520 | 73% |
Reaction Steps
The product from step 1 (4.8 g), thiourea (2.53 g) and potassium methylate (2.33 g) were heated together in boiling propan-2-ol (30 cm3) for 6 hours. The reaction mixture was allowed to cool overnight. The solvent was removed by evaporation under reduced pressure, the residue was dissolved in water and washed with ethyl acetate, the organic layer being discarded. The basic aqueous layer was acidified to pH 5 using glacial acetic acid and the product was extracted into ethyl acetate. Evaporation of the ethyl acetate under reduced pressure gave 3.769 g of an orange oil. 1H NMR (DMSO): δ3.46(6H,s); 5.14(1H,s); 6.94(1H,d); 7.18(1H,br s); 8.18(1H,d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05684011 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-a45f456ecb6e4c128092030274d6b16a |
| Source note | uspto-grants-1997_11 |