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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209547Generated: October 31, 2026

Triphenylphosphine → HCID 57182805, compound

https://huagongshe.com/reaction/2209547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 57285352HCID 57285352—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57182805HCID 5718280583%

Reaction Steps

To a stirred solution of 3.54 g of triphenylphosphine in 50 mL of THF at 0° C. was added 2.66 mL of diisopropyl azodicarboxylate. The mixture was stirred for an additional 30 min. To the resulting white precipitate was added 1.00 g of (2S)-2-(t-butylthio)-1-propanol in 5 mL of THF. The reaction mixture was stirred for 10 min, then 0.966 mL of thiolacetic acid was added and stirring was continued at 0° C. for 1 h and at room temperature for 1 h. The solvent was evaporated under vacuum and the residue was purified by flash chromatography (5% CH2Cl2 in hexane) to give 1.16 g of (2S)-1-(acetylthio)-2-(t-butylthio)propane as an oil at 83% yield. Characteristic analytical data are as follows: 1H NMR (300 MHz, CDCl3) δ3.32 (m, 1H), 2.8-2.94 (m, 2H), 2.35 (s, 3 H), 1.38 (s, 9H), 1.33 (d, J=7 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455262
Source datasetuspto-grants-1995_10
ORD IDord-29e394ee873a4e0aa94ed19cbf17bd57
Source noteuspto-grants-1995_10