HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroacetate → HCID 23315294, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | HCID 13120674 | HCID 13120674 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 23315294 | HCID 23315294 | 83.9% |
Reaction Steps
12 g (0.053 mol) of 3-(2-thienyl)-4-acetylpiperazin-2-one, prepared in accordance with Example 17, are stirred with 6.6 g (0.059 mol) of potassium tert.-butylate in 100 ml of dimethyl sulphoxide. After removing 10 ml of dimethyl sulphoxide by distillation in vacuo, 6.4 g (0.059 mol) of ethylchloroacetate are added dropwise at room temperature and the mixture is stirred for a further 12 hours. The dimethyl sulphoxide is removed by evaporation in vacuo, the residue is stirred with water and taken up in ethyl acetate, and the organic phase is separated off. Distilling off the ethyl acetate gives 13.8 g of the title product, 88% of theory (molecular weight 296), in the form of a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04598079 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-d188686654c64156a8839444dc4f25c7 |
| Source note | uspto-grants-1986_07 |