HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413705Generated: October 31, 2026
Potassium Carbonate → HCID 20290364, compound
https://huagongshe.com/reaction/1413705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | Propanoyl chloride, 3-bromo- | HCID 84944 | — |
| Reactant | 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid | HCID 95489 | — |
| Reactant | Potassium 2-thienylacetate | HCID 23696799 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20290364 | HCID 20290364 | — |
Reaction Steps
To a solution of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (5.0 g., 0.028 M) and sodium hydroxide (2.26 g., 0.056 M) in water (100 ml.) at 10° C. is slowly added 3-bromopropionyl chloride (2.84 ml., 0.028 M). This mixture is stirred at 25° C. overnight. Potassium thiolacetate, prepared by mixing thiolacetic acid (3.00 ml., 0.042 M) and potassium carbonate (3.90 g., 0.028 M) in water (30 ml.), is added to the reaction mixture which is stirred at 25° C. overnight to yield the title compound as an alkali metal salt. Acidification with dilute hydrochloric acid affords the free carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04251444 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-094b24797b8c4ed5acab8167ff82caa2 |
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| Source note | uspto-grants-1981_02 |
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