HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120141Generated: October 30, 2026
Hydrochloric Acid → (2S,3S)-3-[[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methylbutyl]-carbamoyl]oxirane-2-carboxylic acid
https://huagongshe.com/reaction/2120141
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium hydroxide ethanol | HCID 21946426 | — |
| Reactant | [1-(S)-[alpha-(R)-hydroxybenzyl]-3-methylbutyl carbamoyl]oxirane-2-carboxylate | HCID 86585457 | — |
| Product | (2S,3S)-3-[[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methylbutyl]-carbamoyl]oxirane-2-carboxylic acid | HCID 12051469 | — |
Reaction Steps
To a solution of ethyl (2S,3S)-3-[[1-(S)-[α-(R)-hydroxybenzyl]-3-methylbutyl carbamoyl]oxirane-2-carboxylate (558 mg, 1.66 mmol.) in ethanol (4 mL) was dropwise added 0.5N potassium hydroxide/ethanol solution (4.0 mL, 2.0 mmol.) under chilling with ice The mixture was stirred for 4 hours at room temperature, and made acidic to reach pH 1-2 by addition of water (40 m) and 2N hydrochloric acid (approx. 2 mL). The acidic mixture was extracted with three portions of ethyl acetate. The three extracts were combined and washed successively with water and an aqueous saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to give the titled compound as a white amorphous product (490 mg, yield 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689785B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-148a037393904f8baac01f5e6bb49111 |
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| Source note | uspto-grants-2004_02 |
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