HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120144Generated: October 31, 2026
Acetic Anhydride → Ethyl (2S,3S)-3-[[1(S)-[alpha-(R)-acetoxybenzyl]-3-methyl-butyl]carbamoyl]oxirane-2-carboxylate
https://huagongshe.com/reaction/2120144
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl (2S,3S)-3-[[1-(S)-[alpha-(R)-hydroxybenzyl]-3-methyl-butyl]carbamoyl]oxirane-2-carboxylate | HCID 12051467 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl (2S,3S)-3-[[1(S)-[alpha-(R)-acetoxybenzyl]-3-methyl-butyl]carbamoyl]oxirane-2-carboxylate | HCID 12051480 | — |
Reaction Steps
In pyridine (0.6 mL) was dissolved ethyl (2S,3S)-3-[[1-(S)-[α-(R)-hydroxybenzyl]-3-methylbutyl]carbamoyl]-oxirane-2-carboxylate (300 mg, 0.894 mmol.). To the resulting solution was added acetic anhydride (0.085 ML, 0.901 mml.) under chilling with ice. The mixture was stirred for 18 hours at room temperature, and extracted with ether (8 mL, 3 portions) after addition of water (10 mL). The organic portion was washed successively with water, 1N hydrochloric acid, and an aqueous saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1), to give the titled compound as a slightly brownish crystalline product (267 mg, yield: 79%),
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-248343757ecb46e08ad94edae55d3d73 |
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| Source note | uspto-grants-2004_02 |
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