HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209547Generated: October 31, 2026
Triphenylphosphine → HCID 57182805, compound
https://huagongshe.com/reaction/2209547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | HCID 57285352 | HCID 57285352 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57182805 | HCID 57182805 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455262 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-29e394ee873a4e0aa94ed19cbf17bd57 |
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| Source note | uspto-grants-1995_10 |
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