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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754825Generated: October 28, 2026

Triphenylphosphine → HCID 46936097, compound

https://huagongshe.com/reaction/1754825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86646198HCID 86646198—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 46936097HCID 4693609762.2%

Reaction Conditions

Temperature60 °C

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 hr and 60° C. for 3.5 hr. 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169187B2
Source datasetuspto-grants-2015_10
ORD IDord-88a3a8493c2542619e454f929491d1ad
Source noteuspto-grants-2015_10