HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626910Generated: November 1, 2026
Ethanol → Ethyl 2-{[(benzyloxy)carbonyl]amino}-2-methylpropanoate
https://huagongshe.com/reaction/626910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | N-((Benzyloxy)carbonyl)-2-methylalanine | HCID 294936 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-{[(benzyloxy)carbonyl]amino}-2-methylpropanoate | HCID 89649322 | — |
Reaction Steps
To a solution of 2-(benzyloxycarbonylamino)-2-methyl-propanoic acid (which may be prepared as described in Description 32) (5000 mg, 21.08 mmol) in toluene (50 mL) was added ethanol (5 mL) and p-toluenesulfonic acid (400.89 mg, 2.11 mmol). The solution was stirred at 80° C. overnight. The reaction mixture was evaporated and the residues dissolved in EtOAc and washed with saturated aqueous sodium bicarbonate. The aqueous phase was back extracted into EtOAc. The combined organics were dried over magnesium sulphate, filtered and evaporated to yield the title compound (D33) as a light yellow oil (4.667 g);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309254B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-38ecc2c76ad4451e9e7eee9c30d8b720 |
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| Source note | uspto-grants-2016_04 |
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