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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381217Generated: November 3, 2026

HCID 13320303, compound → (3R,4R)-1-Methyl-4-phenoxypyrrolidin-3-ol

https://huagongshe.com/reaction/1381217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13320303HCID 13320303—
CatalystSilver(II) oxideHCID 92152—
SolventEthanolHCID 702—
Product(3R,4R)-1-Methyl-4-phenoxypyrrolidin-3-olHCID 13320201—

Reaction Conditions

Temperature45 °C

Reaction Steps

A solution of 9.3 g. (22.6 mmol.) of trans-3-hydroxy-1-methyl-4-phenoxy-1-phenylmethylpyrrolidinium iodide in 200 ml. of absolute ethanol and 100 ml. of 190 ethanol was stirred at ambient temperature for 0.5 hr. with 2.6 g. (11.3 mmol.) of silver oxide. After 0.2 g. more silver oxide was added, the mixture was warmed to 45° C. and stirred for an additional 15 min. The mixture was separated by filtration through Celite, and the volume of the filtrate was reduced to 200 ml. This solution was treated with ca. 0.5 g. of 10% Pd/C catalyst and was shaken with H2 in the Parr reduction apparatus for 3 hr. The suspension was filtered through Celite and the filtrate was concentrated to give 4.3 g. of crystalline solid. This material, when recrystallized from cyclohexane, gave 3.66 g. (84%) of off-white crystals, m.p. 89.0°-90.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585785
Source datasetuspto-grants-1986_04
ORD IDord-d2e62b66509d468f8d2a54fdb30e4c3d
Source noteuspto-grants-1986_04