HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-dodecyl-2-carbobenzyloxyaminosuccinamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dodecylamine | HCID 13583 | — |
| Reactant | (S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamate | HCID 11128682 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-dodecyl-2-carbobenzyloxyaminosuccinamic acid | HCID 57925483 | 97% |
Reaction Steps
N-Carbobenzyloxy-L-aspartic anhydride (1 mmol) was dissolved in 50 mL methylene chloride, followed by the addition of 1.05 eq of dodecylamine and 1.1 eq of triethylamine. The reaction was capped to prevent evaporation, and stirred for 12 hours. When no trace of starting material could be detected by thin layer chromatography (TLC) (CH2Cl2, 5% MeOH), the reaction was quenched with 20 mL 1N hydrochloric acid followed by extraction with chloroform (5×). The organic layer was dried over magnesium sulfate, and 7 was obtained as a white solid (yield 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138140B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-1401b6324ffe4ff991b4303fe3180ae7 |
| Source note | uspto-grants-2012_03 |