HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230925Generated: October 30, 2026
Hydrochloric Acid → Benzyl 2-amino-2-methylpropanoate hydrochloride
https://huagongshe.com/reaction/230925
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-butyl 2-((benzyloxy)carbonyl)propan-2-ylcarbamate | HCID 23077832 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzyl 2-amino-2-methylpropanoate hydrochloride | HCID 21415531 | — |
Reaction Steps
To a solution of 2-(tert-butoxycarbonylamino)-2-methylpropionic acid (4.06 g) in N,N-dimethylformamide (40 mL) were added potassium carbonate (4.15 g) and benzyl bromide (2.85 mL), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into water, and the resulting mixture was extracted with ethylacetate. The extract was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. The residue (solid) was treated with n-hexane and collected by filtration. The crystals were dried under reduced pressure to give benzyl 2-(tert-butoxycarbonylamino)-2-methylpropionate (4.44 g). To the obtained benzyl 2-(tert-butoxycarbonylamino)-2-methylpropionate (4.44 g) was added 4 mol/L hydrochloric acid (1,4-dioxane solution, 15 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with diethyl ether, and the mixture was stirred for 1 hour. The insoluble material was collected by filtration, washed with diethyl ether and dried under reduced pressure to give the title compound (3.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566699B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-3108d3fe5d494e348c081fabef4ee3d8 |
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| Source note | uspto-grants-2009_07 |
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