HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638415Generated: October 30, 2026
Ethanol → (2-t-Pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylic acid
https://huagongshe.com/reaction/638415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(2-t-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylate | HCID 19978748 | — |
| Reactant | HCID 178473043 | HCID 178473043 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-t-Pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylic acid | HCID 19978737 | — |
Reaction Steps
A mixture of ethyl 2-(2-tert-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-tert-pentyloxycarbonylimino-2,3-dihydro-1,3-thiazol-4-yl)-glyoxylate, (2.8 g.) and ethanol (10 ml.) was mixed with a solution of sodium hydroxide (0.54 g.) in water (20 ml.), and the mixture was stirred for 1 hour at room temperature. After the reaction, a small amount of ethanol was distilled off. The remaining reaction mixture was washed with diethyl ether and then the aqueous layer was separated therefrom. To the aqueous layer was added ethyl acetate, and the mixture was adjusted to pH 1 to 2 with 10% hydrochloric acid and then the ethyl acetate layer was separated therefrom. The ethyl acetate layer was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and then treated with activated charcoal. The solvent was distilled off from the ethyl acetate layer to give yellow brown powder of 2-(2-tert-pentyloxycarbonylamino-1,3-thiazol-4-yl)glyoxylic acid, which can be represented as 2-(2-tert-pentyloxycarbonylimino-2,3-dihydro-1,3-thiazol-4-yl)glyoxylic acid, (1.75 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04560765 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-54f3f964cb4a48d9b6ec94fba882072a |
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| Source note | uspto-grants-1985_12 |
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