HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Phenylalanine → 2-[(2-naphthylsulfonyl)amino]-3-phenylpropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(2-naphthylsulfonyl)amino]-3-phenylpropanoic acid | HCID 3125909 | — |
Reaction Steps
A solution of 7.6 mmol (1.71 g) of 2-naphthylsulphonyl chloride in 10 ml of dichloromethane and a solution of 7.9 mmol (0.32 g) of sodium hydroxide in 10 ml of water are added slowly in succession to 7.6 mmol (1.25 g) of phenylalanine and 7.6 mmol (0.3 g) of sodium hydroxide in 10 ml of water. The reaction mixture is stirred for 1 hour at room temperature. After decanting, the aqueous phase is washed with dichloromethane and rendered acidic to pH=2 with a dilute hydrochloric acid solution. After extraction with dichloromethane, the organic phase is dried over sodium sulphate and concentrated to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271247B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-02834b612f2b477595d0e817fdc892f0 |
| Source note | uspto-grants-2001_08 |