HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl 2,2,2-Trichloroacetimidate → HCID 13995645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl 2,2,2-Trichloroacetimidate | HCID 316905 | — |
| Reactant | N-((Phenylmethoxy)carbonyl)-L-serine methyl ester | HCID 6999535 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Dichloromethane cyclohexane | HCID 21916607 | — |
| Product | HCID 13995645 | HCID 13995645 | — |
Reaction Steps
Dissolve N-(benzyloxycarbonyl)-L-serine methyl ester (63 mmol) in methylene chloride/cyclohexane (1:1, 600 mL). Add allyl trichloroacetimidate (26 g, 128 mmol) and trifluroromethanesulfonic acid (5 mL, 56.6 mmol). Stir at room temperature under a nitrogen atmosphere for 5 hours and dilute with methylene chloride. Wash with saturated aqueous sodium hydrogen carbonate, water, dry (MgSO4) and evaporate the solvent in vacuo. Purify by silica gel chromatography to give N-(benzyloxycarbonyl)-O-2-propenyl-L-serine methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05635502 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-68d19dc374a24a92a449feea2e3b0a90 |
| Source note | uspto-grants-1997_06 |