HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024902Generated: October 29, 2026
Ethyl Acetate → (2S,3R)-3-(Benzyloxy)-2-hydroxybutanoic acid
https://huagongshe.com/reaction/1024902
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | O-BENZYL-L-THREONINE | HCID 6951054 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | (2S,3R)-3-(Benzyloxy)-2-hydroxybutanoic acid | HCID 67051262 | — |
Reaction Steps
To a solution of (2S,3R)-2-amino-3-benzyloxy-butyric acid (1.1 g) in 2M sulfuric acid (6.31 mL) was added dropwise over 2 h a solution of sodium nitrite (0.65 g) in water (6 mL), keeping the internal temperature of the reaction below 0° C. The reaction mixture was stirred at −5° C. for 6 h then allowed to warm to room temperature overnight. The mixture was adjusted to pH 4 with 50% aqueous sodium hydroxide then ethyl acetate was added. The mixture was stirred vigorously and acidified to pH 2 with concentrated sulfuric acid. The layers were separated and the aqueous layer extracted with further ethyl acetate (×2). The combined organic extracts were washed with saturated aqueous sodium chloride, dried (MgSO4), filtered and evaporated to give the subtitle compound as a yellow crystalline solid which was used without further purification. Yield: 0.84 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722883B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-480cd663eec74dc2a0b06b834fad68c8 |
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| Source note | uspto-grants-2014_05 |
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