HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902700Generated: October 26, 2026
Triphenylphosphine → HCID 69252373, compound
https://huagongshe.com/reaction/902700
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | tert-Butyl 4-(3-hydroxyphenyl)piperazine-1-carboxylate | HCID 18669061 | — |
| Reactant | 3-[(2-Chloro-3-trifluoromethyl-benzyl)-diphenylethyl-amino]-propan-1-ol | HCID 57757117 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69252373 | HCID 69252373 | 84% |
Reaction Steps
To a stirring solution of 3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propan-1-ol (448 mg, 1.0 mmol) in toluene (30 mL) was added 4-(3-hydroxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (419 mg, 1.50 mmol). Polymer bound triphenylphosphine (500 mg, 1.50 mmol, 3 mmol/g, Fluka Chemie) was then added, and the mixture stirred for 15 minutes. The reaction mixture was then cooled to 0° C. and diisopropylazodicarboxylate (303 mg, 1.50 mmol) was added in a dropwise fashion. After stirring at room temperature overnight, the crude reaction mixture was filtered and the solid washed with toluene. Concentration of the filtrate in vacuo followed by purification by flash silica gel chromatography (silica gel 60, EM science; 15% EtOAc:hexane) afforded title compound as an oil (0.59 g, 84%). MS(ES) m/e 708.4 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365085B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-66198db799b84ca5a66e43faee1ac1b2 |
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| Source note | uspto-grants-2008_04 |
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