HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 13373610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Benzyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate | HCID 11594288 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13373610 | HCID 13373610 | — |
Reaction Steps
Dissolve 7.0 g of 1-benzyloxycarbonyl-4-keto-(S)-proline methyl ester in 75 ml of glacial acetic acid. Add 0.7 g of p-toluenesulfonic acid and 2.8 g of 1,2-ethanedithiol and heat under reflux with stirring for eighteen hours. Add the reaction mixture to saturated sodium bicarbonate solution and extract with ethyl acetate. Dry the organic layer over magnesium sulfate and concentrate it. Place the residue on a column of silica gel (300 g, 60-200 mesh) and elute with hexane:ethyl acetate (1:1) to give 7-benzyloxycarbonyl-1,4-dithia-7-azaspiro-[4.4]nonane-8(S)-carboxylic acid methylester, a yellow oil having [α]D26 -12.6° (dioxane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04470972 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-8fc17723cfe94c3688b50ae9719afe57 |
| Source note | uspto-grants-1984_09 |