HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-[N-benzyloxycarbonyl-(S)-alanyl]hexhydrofuro[3,4-b]pyrrole-2(S)-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-[N-benzyloxycarbonyl(S)-alanyl]hexahydrofuro[3,4-b]pyrrole-2(S)-carboxylic acid, ethyl ester | HCID 86748148 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[N-benzyloxycarbonyl-(S)-alanyl]hexhydrofuro[3,4-b]pyrrole-2(S)-carboxylic acid | HCID 18654884 | — |
Reaction Steps
To a solution of 1 -[N-benzyloxycarbonyl- (S) -alanyl]hexahydrofuro[3,4 -b]pyrrole-2(S)-carboxylic acid, ethyl ester in methanol, add 2.5 N sodium hydroxide and stir the mixture at room temperature for 18 hours. Concentrate the mixture under nitrogen, dilute the residue with ice-water and then make the mixture acidic with concentrated hydrochloric acid. Extract the aqueous solution with ethyl acetate and dry the organic phase over magnesium sulfate. Concentrate the organic phase and place it on a column of silica gel. Elute with chloroform:glacial acetic acid 9:1 to give 1-[N-benzyloxycarbonyl-(S)-alanyl]hexahydrofuro[3,4-b ]pyrrole-2(S)-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05348944 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-f3168b1de05b42f1bc4b5eb7eb2f502a |
| Source note | uspto-grants-1994_09 |