HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859953Generated: October 27, 2026
Hydrochloric Acid → 2-Tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylic acid
https://huagongshe.com/reaction/859953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl-2-tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate | HCID 21911455 | — |
| Solvent | 2-(Oxolan-2-yl)ethan-1-ol | HCID 11989572 | — |
| Product | 2-Tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylic acid | HCID 21911430 | — |
Reaction Steps
A stirred solution of ethyl-2-tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate (10 g, 34.95 mmol) in tetrahydrofuran-ethanol (250 mL, 2:3) was treated with a 6N KOH solution (250 mL). The mixture was heated to 55° C. overnight. The solution was cooled to 0° C. and acidified with concd. HCl to pH 1. The solvent was evaporated in vacuo. The residue was washed with water, diethyl ether, dried in vacuo over anhydrous phosphorous pentoxide to obtain the title acid (6 g, 89%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153856B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-a8bc5320631e42c1bd8849e7c01ef65a |
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| Source note | uspto-grants-2006_12 |
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