HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Phenylalanine → HCID 66991917, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57507304 | HCID 57507304 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 66991917 | HCID 66991917 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To an aqueous solution of NaOH (1N, 10 mL) at 0° C. was added L-2-amino-3-phenyl-propionic acid (1.47 g, 8.92 mmol), followed by the addition of solution of 3,6-dichloro-3-(3-chloro-benzyl)-1,3-dihydro-indol-2-one (3 g, 8.1 mmol) in 1,4-dioxane (3 mL). After the reaction mixture was stirred at 0° C. for 4 h, the solution was concentrated and extracted with diethyl ether. The organic layer was dried over Na2SO4, filtered and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058269B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-c4b96074d0d34ef38d4fd92f93d2b248 |
| Source note | uspto-grants-2011_11 |