HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296605Generated: November 1, 2026
Ethyl Thioglycolate → HCID 18387351, compound
https://huagongshe.com/reaction/2296605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Thioglycolate | HCID 12185 | — |
| Reactant | HCID 527701 | HCID 527701 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Allyl Alcohol | HCID 7858 | — |
| Product | HCID 18387351 | HCID 18387351 | 88.1% |
Reaction Steps
Sodium (9.06 g; 0.39 mole) was decomposed in allyl alcohol (380 ml). The obtained solution was treated by dropwise adding of first ethyl mercaptoacetate (42.7 ml; 0.39 mole) at the temperature of 0° C. and then of allyl 4-chlorobutyrate (58.3 g; 0.36 mole) prepared according to the process disclosed in Example 2a. The obtained mixture was stirred for three hours at room temperature and then for 1 hour at reflux temperature. The mixture was concentrated by evaporation and poured into a mixture of diethylether (200 ml) and of an ice/water mixture (100 g). The obtained solution was acidified with 1M hydrochloric acid solution to achieve a pH value of the medium between 3 and 6. The ether phase was separated and the obtained aqueous phase was extracted with diethyl ether (200 ml). The combined ether fractions were washed with water (200 ml) and 4% aqueous sodium hydrogencarbonate solution (200 ml) and dried with magnesium sulfate. After the removal of the drying agent and evaporation of ether, the title compound (78.1 g; 84%) was obtained, which was used in the crude form in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06489318B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-6529ee5d522d482bb354817a8784bd4b |
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| Source note | uspto-grants-2002_12 |
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