HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl {[2-(1,3-benzodioxol-5-yl)-2-oxoethyl]thio}acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | 1-(1,3-Dioxaindan-5-yl)-2-bromoethan-1-one | HCID 243777 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl {[2-(1,3-benzodioxol-5-yl)-2-oxoethyl]thio}acetate | HCID 43218502 | — |
Reaction Steps
Ethyl 2-mercaptoacetate (9.68 mL, 88.3 mmol) was added dropwise to a suspension of K2CO3 (12.2 g, 88.3 mmol) and 1-(1,3-benzodioxol-5-yl)-2-bromoethanone (21.4 g, 88.3 mmol) in dry acetone (100 mL). The mixture was stirred at reflux for seven hours, cooled at an icebath and added 200 mL water. Diethyl ether (400 mL) was added and the phases were separated. The aqueous layer was extracted with diethyl ether (200 mL) and the combined organic layers were washed with brine (200 mL), dried (MgSO4) and concentrated. This afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07906502B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-00a960acb4124e9db5ade53abf3de7aa |
| Source note | uspto-grants-2011_03 |