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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742699Generated: November 2, 2026

Methyl p-toluenesulfonate → 3-Pyrrolidinol, 1-[(4-methylphenyl)sulfonyl]-, 3-(4-methylbenzenesulfonate), (3S)-

https://huagongshe.com/reaction/1742699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(3R)-1-(4-Methylbenzene-1-sulfonyl)pyrrolidin-3-olHCID 16216944—
SolventTetrahydrofuranHCID 8028—
Product3-Pyrrolidinol, 1-[(4-methylphenyl)sulfonyl]-, 3-(4-methylbenzenesulfonate), (3S)-HCID 44248020—

Reaction Conditions

Temperature-20 °C

Reaction Steps

Methyl para-toluenesulphonate (54 g) was added in portions to solution of 1-tosyl-3-(R)-(-)-hydroxypyrrolidine (49 g--see Preparation 2) and triphenylphosphine (76 g) in anhydrous tetrahydrofuran (700 ml) at 0° C. The mixture was cooled to -20° C. and diethyl azodicarboxylate (58 g--"DEAD") was added, dropwise, over 30 minutes. During this time, the temperature of the mixture was not allowed to rise above -10° C. When the addition was complete the mixture was allowed to warm to room temperature and stirred for 16 hours. The mixture was concentrated in vacuo to give a solid which was purified by column chromatography on silica eluting with hexane containing dichloromethane (50%). The product-containing fractions were combined and concentrated in vacuo to give an oil which was crystallised from 1-propanol to give the title compound as a colourless solid, yield 56 g, m.p. 110° C., [α]25D -5.2° (c 1.0, CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05340831
Source datasetuspto-grants-1994_08
ORD IDord-9b4f38cadc4441919bf40ed72fe9c097
Source noteuspto-grants-1994_08