HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978623Generated: October 29, 2026
Thioglycolic Acid → HCID 13176140, compound
https://huagongshe.com/reaction/978623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioglycolic Acid | HCID 1133 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Hydroxy-4-methyl-5-(prop-2-en-1-yl)cyclopent-2-en-1-one | HCID 12879872 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13176140 | HCID 13176140 | 90.7% |
Reaction Steps
Into the same flask as used in Example 1, triethylamine (10 g), mercaptoacetic acid (30 g) and toluene (50 g) were charged, and 2-allyl-3-hydroxy-3-methyl-4-cyclopentenone (15.2 g) was dropwise added thereto at a temperature of 20° to 40° for 1 hour. Thereafter, the reaction mixture was stirred at a temperature of 50° to 70° C. for 4 hours. After completion of the reaction, the mixture was evaporated under reduced pressure. The residue was dissolved in a 5% aqueous solution of sodium bicarbonate (100 g), and undissolved materials were filtered off. The filtrate was treated with an acid and extracted with diethyl ether. Diethyl ether was evaporated off from the organic layer to obtain 2-allyl-3-methyl-4-carboxymethylthio-2-cyclopentenone (20.5 g). Yield, 90.5%. nD20 1.5567.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04665174 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-031164763acb4af98ee7e4a90e1fb77e |
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| Source note | uspto-grants-1987_05 |
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