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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291831Generated: November 2, 2026

Triphenylphosphine → HCID 14154745, compound

https://huagongshe.com/reaction/2291831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(+-)-3-QuinuclidinolHCID 15381—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
CatalystSodium HydroxideHCID 14798—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14154745HCID 14154745—

Reaction Conditions

Temperature5 °C

Reaction Steps

Diisopropyl azodicarboxylate (31.6 cc) is added dropwise in the course of 30 minutes to a solution, maintained at 5° C. under an atmosphere of nitrogen, of triphenylphosphine (42 g) in tetrahydrofuran (300 cc). The suspension obtained in then stirred for 30 minutes at 5° C. A solution of 3-hydroxyquinuclidine (10.2 g) and thiolacetic acid (11.4 cc) in tetrahydrofuran (600 cc) is then added to this suspension, maintained at 5° C., in the course of 30 minutes. The reaction mixture is then stirred for 20 hours at a temperature in the region of 20° C. It is then concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. The oil obtained is dissolved in ethyl ether (400 cc), and then washed with hydrochloric acid (3×160 cc). The combined aqueous phases are washed with ethyl ether (100 cc) and then neutralized to a pH in the region of 7 by adding sodium bicarbonate. The pH of the solution obtained is then adjusted to about 9 by adding a few drops of 10N aqueous sodium hydroxide solution. The mixture is extracted with methylene chloride (3×200 cc). The combined organic phases are dried over sodium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa) at 30° C. 3-(Acetylthio)quinuclidine (14.7 g) is thereby obtained in the form of a brown oil [Rf=0.33; eluant: methylene chloride/methanol (90:10 by volume)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798827
Source datasetuspto-grants-1989_01
ORD IDord-26d5265a99ac4aa7b9d7544174bb9ca8
Source noteuspto-grants-1989_01