HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(benzylsulfonyl)-D-isoleucyl-L-methionine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl ester | HCID 69623705 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-(benzylsulfonyl)-D-isoleucyl-L-methionine | HCID 69623728 | 100% |
Reaction Steps
To a solution of N-(benzylsulfonyl)-D-isoleucyl-L-methionine methyl ester (6.4 g, 14.9 mmol) in ethanol (30 ml), 2N aqueous sodium hydroxide (30 ml) was added and stirred at room temperature. After 1 hour, the reaction mixture was adjusted to pH 2 with 2N aqueous hydrogen chloride and then extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine and then dried over anhydrous magnesium sulfate. Magnesium sulfate was filtered off and the filtrate was concentrated under reduced pressure to give N-(benzylsulfonyl)-D-isoleucyl-L-methionine (6.2 g, 14.9 mmol; yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07001887B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-f200889d87434159b73a781ca6fa1ad2 |
| Source note | uspto-grants-2006_02 |