HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398755Generated: November 1, 2026
Ethanol → Ethyl 2-(2-thioxo-2,3-dihydrobenzoxazol-5-yl)propionate
https://huagongshe.com/reaction/2398755
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Reactant | Ethyl 3-amino-4-hydroxy-phenyl-propionate | HCID 12202638 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-(2-thioxo-2,3-dihydrobenzoxazol-5-yl)propionate | HCID 20319623 | — |
Reaction Steps
A stirred mixture of ethyl 2-(3-amino-4-hydroxyphenyl)propionate (8.4 g.), potassium ethylxanthate (6.33 g.), ethanol (38 ml.) and water (6.5 ml.) was heated under reflux for 4 hours. The solution was evaporated to half volume and diluted with water (65 ml.). The mixture was acidified with 2N-hydrochloric acid and extracted several times with ether. The ethereal solution was washed with water, then dried with anhydrous sodium sulphate, and evaporated to give ethyl 2-(2-thioxo-2,3-dihydrobenzoxazol-5-yl)propionate as an oil. Dry chlorine was passed into a solution of the thione (9 g.) in freshly dried and distilled chloroform (150 ml.) with stirring for 4 hours. The solution was then washed with water, N-sodium hydroxide solution, then water (3x). The dried (Na2SO4) organic solution was evaporated to yield ethyl 2-(2-chloro-5-benzoxazolyl)propionate as a brown oil which was shown to be a single compound by thin layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04025637 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-1e2d7341631b4b839569e65bb8344a18 |
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| Source note | uspto-grants-1977_05 |
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