HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Thioglycolate → 5-(Carbethoxymethylthio)-1-(2-furyl)-1-pentanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 5-Chloro-1-(2-furyl)-1-pentanol | HCID 20292579 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(Carbethoxymethylthio)-1-(2-furyl)-1-pentanol | HCID 20292574 | — |
Reaction Steps
To a stirred, refluxing mixture of 76 g of ethyl mercaptoacetate, 79.5 g of 5-chloro-1-(2-furyl)-1-pentanol (Example), and 10 ml of 1.5 M sodium ethoxide in ethanol is added an additionan 300 ml of 1.5 M sodium ethoxide during 15 minutes. The resulting mixture is stirred at reflux for 3 hours, cooled, and concentrated to remove most of the ethanol. The residue is partitioned with ether and water. The ether phase is washed with brine and dried over potassium carbonate. The solution is concentrated, diluted with xylene, and again concentrated to give an oil, pmr spectrum (CDCl3): δ3.24 (singlet, --S--CH2CO2C2H5) and 4.70 (triplet, CH2CHOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04245121 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-e291fa8fd5f74f74babd6105a3df202a |
| Source note | uspto-grants-1981_01 |