HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080549Generated: October 30, 2026
Triphenylphosphine → HCID 86646579, compound
https://huagongshe.com/reaction/2080549
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 86646578 | HCID 86646578 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86646579 | HCID 86646579 | 63.5% |
Reaction Steps
To a stirred, cold (0° C.) solution of 3.11 grams (0.012 mole) of triphenylphosphine in 200 mL of THF was added dropwise 2.28 grams (0.011 mole) of diisopropyl azodicarboxylate. The reaction mixture was stirred at 0° C. for five hours and at that time a solution of 1.37 grams (0.0056 mole) of 2-{[(6-chloro(3-pyridyl))methyl](2-methylpropyl)amino}ethan-1-ol and 0.94 gram (0.012 mole) of thiolacetic acid in 50 mL of THF was added dropwise. After complete addition the reaction mixture was stirred at 0° C. for one hour. The reaction mixture was concentrated under reduced pressure to a residue. The residue was purified by column chromatography on silica gel, eluting with mixtures of n-heptane and ethyl acetate. The appropriate fractions were combined and concentrated under reduced pressure, yielding 1.07 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932393B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-d0c315c473f04727bb2d90814df7281d |
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| Source note | uspto-grants-2011_04 |
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