HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908654Generated: November 1, 2026
Triphenylphosphine → HCID 59366521, compound
https://huagongshe.com/reaction/908654
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-[3-(Trifluoromethyl)phenyl]-2H-tetrazole | HCID 706933 | — |
| Reactant | HCID 22006767 | HCID 22006767 | — |
| Product | HCID 59366521 | HCID 59366521 | 112.7% |
Reaction Steps
Diisopropyl azodicarboxalate (0.056 gram, 0.00028 mole) was added to a stirred, cold (0° C.) mixture of 0.072 gram (0.00028 mole) of triphenylphosphine, 0.045 gram (0.00021 mole) of 5-(3-trifluoromethylphenyl)-2H-1,2,3,4-tetrazole and 0.075 gram (0.00023 mole) of 2-(4-(3,3-dichloroprop-2-enyloxy)-2,6-dichlorophenoxy)ethan-1-ol. The cold reaction mixture stirred for one hour at which time the mixture was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel, eluting with hexanes:ethyl (80:20). The appropriate fractions were combined and concentrated under reduced pressure to yield 0.125 gram of an oil. This oil was combined with similarly obtained oils from three reactions preformed in a similar manner. The combined oil was further purified by column chromatography on silica gel, eluting with mixtures of hexanes, methylene chloride and ethyl acetate to yield 0.267 gram of the subject compound as an oil. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017635B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-c220de6c9c4d4d3c92a98a3bdce12c11 |
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| Source note | uspto-grants-2011_09 |
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