HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486726Generated: October 30, 2026
Triphenylphosphine → HCID 54295485, compound
https://huagongshe.com/reaction/486726
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 54267952 | HCID 54267952 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54295485 | HCID 54295485 | 82% |
Reaction Steps
To a stirred solution of triphenylphosphine (391 mg) in THF (3 ml), azodicarboxylic acid diethylester (260 mg) dissolved in THF (1 ml) was added at -15°--10° C. under nitrogen atmosphere. To the mixture, trans-4-tert-butoxycarbonyl-2-hydroxymethyltetrahydrothiophene (compound No. 1-1, 150 mg) and thioacetic acid (114 mg) dissolved in THF (2 ml) were added at -20°--15° C., and the mixture was stirred for 1 hour at -20° C. and for 1 hour at room temperature. The mixture was concentrated in vacuo. The oily residue was purified by a silica gel column chromatography to give 169 mg (82%) of the titled compound (compound No. 4-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292767 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-72410ae4e29f412b9bb724956c418a05 |
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| Source note | uspto-grants-1994_03 |
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