HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469868Generated: October 25, 2026
Tert-Butyl nitrite → (S)-2-Acetoxybutanoic acid
https://huagongshe.com/reaction/1469868
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | (-)-2-Aminobutyric acid | HCID 80283 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (S)-2-Acetoxybutanoic acid | HCID 13327295 | 60% |
Reaction Steps
Sodium acetate (11.9 g, 146 mmol) and tert-butyl nitrite (15.0 g, 146 mmol) were added to an acetic acid (300 mL) solution of (2S)-2-aminobutyric acid (10.0 g, 97.0 mmol) under ice cooling, and was stirred at 60° C. for 2 hours. The reaction mixture was cooled to room temperature, and then the solvent was distilled off under reduced pressure. Water was added to the residue, and the mixture was subjected to extraction twice with ethyl acetate. The organic layer thus obtained was washed with water and brine, and then was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. Furthermore, the residue was azeotropically boiled with 1,4-dioxane (50 mL) twice. Thus, the title compound (8.4 g, yield: 60%) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006273B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-b6b169fe7a934fdfb1416952db2aa9cf |
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| Source note | uspto-grants-2015_04 |
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