HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918280Generated: October 30, 2026
Ethyl Thioglycolate → HCID 20364852, compound
https://huagongshe.com/reaction/918280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 5826656 | HCID 5826656 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20364852 | HCID 20364852 | — |
Reaction Steps
The starting material is prepared as follows: 8.65 g of ethyl 4,4-diethoxycrotonate are added at once at 0° to the mixture prepared from 1 g of pulverized sodium, 40 ml of ethanol and 4.94 ml of ethyl thioglycolate, evaporating the mixture after stirring it at room temperature and adding 43 ml of dimethylsulfoxide and 20 ml of dimethylformamide. The mixture is stirred at 0° for 1/2 hour and at room temperature for 2 hours, poored into cold water and extracted with diethyl ether. The aqueous layer is acidified with 21.7 ml of cold 2N hydrochloric acid and extracted with diethyl ether. The extract is dried and evaporated, to yield the ethyl 2-diethoxymethyl-4-oxo-tetrahydrothiophene-3-carboxylate showing in the Ir spectrum-bands at 1750, 1725, 1660, 1615 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03970670 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-3052f7103ffa4895a8d61ab5a01131c9 |
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| Source note | uspto-grants-1976_07 |
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