HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 58868954, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | HCID 58868931 | HCID 58868931 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58868954 | HCID 58868954 | — |
Reaction Steps
1.0 ml (6.01 mmol) of trifluoromethanesulfonic anhydride is added dropwise to a solution of 2.27 g (5.46 mmol) of benzyl N-(tert-butoxycarbonyl)-3-hydroxy-6-nitro-L-phenylalaninate (Example 12I) and 1.52 ml (10.9 mmol) of triethylamine in 150 ml of dichloromethane at −15° C. (acetone/dry ice bath). After 15 min, the mixture is warmed to RT, and water is added. The organic phase is separated, washed several times with water, dried over magnesium sulfate and concentrated in vacuo. The crude product is purified by RP-HPLC (mobile phase: acetonitrile/water gradient).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07655643B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-e05686c2bd274fb4bc67cfc305157731 |
| Source note | uspto-grants-2010_02 |