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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941715Generated: November 4, 2026

Triphenylphosphine → HCID 86633581, compound

https://huagongshe.com/reaction/1941715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 23436794HCID 23436794—
SolventAcetonitrileHCID 6342—
ProductHCID 86633579HCID 86633579—
ProductHCID 86633581HCID 86633581226.1%

Reaction Steps

Both compounds, Mito-Gd-DOTA (FIG. 16-4) and Mito-Gd-DTPA, were synthesized according the synthetic route shown in FIG. 16. (10-aminodecyl)triphenylphosphonium bromide (FIG. 16-3) was synthesized and prepared as previously described. Briefly, a mixture containing (10-bromodecyl)phthalimide (7 g, 0.019 mol) and triphenylphosphine (5 g, 0.019 mol) in acetonitrile (60 mL) was refluxed for 15 hours. The solvent distilled under reduced pressure. Purification of the crude product by flash chromatography on a silica gel (CH2Cl2/EtOH 80:20) afforded a white solid 10-decylphthalimidyl triphenylphosphonium bromide (9 g, 73%). The calculated MS value for [C36H39NO2P]+, Br−; [C36H39NO2P]+ is 548.3. the product's MS value was 548.3. To prepare the (10-aminodecyl)triphenylphosphonium bromide (FIG. 16-3), hydrazine was added (0.54 mL, 0.0108 mol) to a solution of (10-decylphthalimidyl)triphenylphosphonium bromide (7 g, 0.0108 mol) in EtOH (70 mL). The mixture was refluxed for 15 hours. The solvent was removed under reduced pressure and the impurity was crystallized using a mixture Et2O/EtOH (100 mL+45 mL). The product was purified by flash chromatography on a silica gel (CH2Cl2/EtOH 80:20) afforded a yellow solid (4 g, 73%). The calculated HRMS for [C28H37NP]+, Br−; [C28H37NP]+ is 418.2. The product's measured HRMS value was 418.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08388936B2
Source datasetuspto-grants-2013_03
ORD IDord-d71e6e727d924c1aae66a2943af11121
Source noteuspto-grants-2013_03