HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496184Generated: November 1, 2026
Aminoisobutyric acid → HCID 22313664, compound
https://huagongshe.com/reaction/496184
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | 2-Acetoxybenzoyl chloride | HCID 79668 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22313664 | HCID 22313664 | — |
Reaction Steps
To a solution of 2-(chlorocarbonyl)phenyl acetate (20 mmol, 3.96 g) in toluene (50 ml) were N-ethyl-N,N-diisopropylamine (22 mmol, 2.84 g) and 2-methylalanine (22 mmol, 2.27 g) added. After stirring the reaction mixture at room temperature overnight, the mixture was diluted with 250 ml toluene and was washed with 1.8% HCl/aq (250 ml) and sat. NaCl/aq (250 ml). The organic phase was dried over Na2SO4 and concentrated under reduced pressure. The residue was dissolved in MeOH (50 mL) and 3 drops of conc. H2SO4 were added. The mixture was refluxed for 2 hours and concentrated under reduced pressure. The residue was dissolved in 250 mL EtOAc and washed with sat.NaHCO3/aq (250 ml) and sat. NaCl/aq (250 ml). The organic phase was dried over Na2SO4 and concentrated at reduced pressure. The resulting crude material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06943188B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-2f1222094bdb4ddfa7c4d99a2decd457 |
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| Source note | uspto-grants-2005_09 |
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