HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025050Generated: November 2, 2026
Triphenylphosphine → HCID 46936097, compound
https://huagongshe.com/reaction/1025050
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86646198 | HCID 86646198 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 46936097 | HCID 46936097 | 62.2% |
Reaction Steps
To azido-bis[4-(12-docosoxydodecyloxy)phenyl]methane (72.0 mg, 58.7 μmol) were added toluene (2 ml), purified water (2 ml), and triphenylphosphine (29 mg, 110 μmol), and the mixture was vigorously stirred at 45° C. for 3 hours and 60° C. for 3.5 hours. The reaction mixture was cooled to room temperature, and 10% aqueous sodium hydrogen carbonate (2 ml) was added. After stirring for a while, toluene (8 ml) was added and the aqueous layer was discarded. The organic layer was washed with purified water (10 ml)×2. The organic layer was evaporated under reduced pressure, and the residue was crystallized from acetonitrile, and the obtained crystals were washed with purified water to give amino-bis[4-(12-docosoxydodecyloxy)phenyl]methane (44 mg, 36.5 μmol, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722934B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-02578e9f1c1d49ddaa918eb4b61cc226 |
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| Source note | uspto-grants-2014_05 |
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