Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | N-carbomethoxy-L-alanine | HCID 13048344 | — |
Reaction Steps
L-Alanine (2.0 g, 22.5 mmol) was dissolved in 10% aqueous sodium carbonate solution (50 mL), and a THF (50 mL) solution of methyl chloroformate (4.0 mL) was added to it. The reaction mixture was stirred under ambient conditions for 4.5 hours and concentrated in vacuo. The resulting white solid was dissolved in water and acidified with 1N HCl to a pH ˜2-3. The resulting solutions was extracted with ethyl acetate (3×100 mL), and the combined organic phase was dried (Na2SO4), filtered, and concentrated in vacuo to provide a colorless oil (2.58 g). 500 mg of this material was purified by a reverse phase HPLC(H2O/methanol/TFA) to provide 150 mg of Cap-12 as a colorless oil. 1H NMR (DMSO-d6, δ=2.5, 500 MHz) 7.44 (d, J=7.3, 0.8H), 7.10 (br s, 0.2H), 3.97 (m, 1H), 3.53 (s, 3H), 1.25 (d, J=7.3, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362020B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-c8dbd5fa9d05456fb39f3c91e7341b59 |
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| Source note | uspto-grants-2013_01 |
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