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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656690Generated: November 2, 2026

Triphenylphosphine → HCID 14154745, compound

https://huagongshe.com/reaction/1656690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant(+-)-3-QuinuclidinolHCID 15381—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14154745HCID 1415474571%

Reaction Steps

To a THF (300 mL) solution of triphenylphosphine (42 g, 160 mmol, 2 equiv) at 0° C. was added diisopropyl azodicarboxylate (32 mL, 162 mmol) to produce a pale yellow solid. A THF (300 mL) solution of 3-quinuclidinol (10.2 g, 80.2 mmol) and thiolacetic acid was added dropwise to the yellow reaction mixture and stirred overnight. THF was removed in vacuo and the residue was dissolved in ether (500 mL) and extracted with 10% HCl (4×150 mL). The aqueous acidic phase was back extracted with ether/ethyl acetate (75 mL/25 mL) and then neutralized to pH 7 by the addition of sodium bicarbonate cautiously in small portions. The aqueous layer was then basified to pH 9-10 by adding a few drops of 10N NaOH, then extracted with dichlormethane (5×200 mL), dried over anhydrous sodium sulfate and concentrated. Purification by flash column chromatrography using 5% MeOH in chloroform as eluent gave 3-acetylthioquinuclidine (10.5 g, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254682
Source datasetuspto-grants-1993_10
ORD IDord-8400fa138ca045729ea8b0783ad1d2bc
Source noteuspto-grants-1993_10