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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249679Generated: October 29, 2026

benzyl (2S,4R)-2-(4-methyl-1-pentenyl)-4-[(2-methyl-2-propenyl)oxy]-1-pyrrolidinecarboxylate → (2R,4R)-4-isobutoxy-2-(4-methylpentyl)pyrrolidine

https://huagongshe.com/reaction/2249679

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl (2S,4R)-2-(4-methyl-1-pentenyl)-4-[(2-methyl-2-propenyl)oxy]-1-pyrrolidinecarboxylateHCID 86630055—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product(2R,4R)-4-isobutoxy-2-(4-methylpentyl)pyrrolidineHCID 6898493897.6%

Reaction Steps

In 5.8 ml of ethanol is dissolved 0.29 g of benzyl (2S,4R)-2-(4-methyl-1-pentenyl)-4-[(2-methyl-2-propenyl)oxy]-1-pyrrolidinecarboxylate. After adding 0.06 g of 5% palladium-carbon, the mixture is stirred at ambient temperature for 1.5 hours in a stream of hydrogen. The reaction mixture is filtered with Celite, and the solvent is distilled off from the filtrate under reduced pressure. Thus, 0.18 g of (2R,4R)-4-isobutoxy-2-(4-methylpentyl)-pyrrolidine is obtained as a yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-095370c973924051848badfe28e495d7
Source noteuspto-grants-2008_01