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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417768Generated: October 27, 2026

p-Toluenesulfonic acid → HCID 13373610, compound

https://huagongshe.com/reaction/2417768

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1,2-EthanedithiolHCID 10902—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Benzyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylateHCID 11594288—
SolventAcetic AcidHCID 176—
ProductHCID 13373610HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04470972
Source datasetuspto-grants-1984_09
ORD IDord-8fc17723cfe94c3688b50ae9719afe57
Source noteuspto-grants-1984_09