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| Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II) Basic information | | Physical Form Reaction |
| Product Name: | Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II) | | Synonyms: | Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II);P(tBu)3 Pd G2;Chloro(tri-t-butylphosphine)(2'-amino-1,1'-biphenyl-2-yl)palladium(II);Chloro[(tri-tert-butylphosphine)-2'-amino[1,1'-biphenyl]-2-yl]palladium(II);Chloro[(tri-t-butylphosphine)-2-(2-aminobiphenyl)]palladium(II);Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II);tBu3PPdG2 catalyst;Chloro(tri-t-butylphosphine)(2'-amino-1,1'-biphenyl-2-yl)palladium(II), min. 98% | | CAS: | 1375325-71-5 | | MF: | C24H37ClNPPd | | MW: | 512.41 | | EINECS: | | Product Categories: | Pd | | Mol File: | 1375325-71-5.mol |
| Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II) Chemical Properties |
| Melting point | 158-160°C | | form | Powder | | color | yellow | | InChIKey | CCFGXRYKSYUWKT-UHFFFAOYSA-N |
| Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II) Usage And Synthesis |
| Physical Form | Yellow powder | | Reaction | Catalyst for the Suzuki Coupling of brominated 2,1-borazaronaphthalenes and potassium organotrifluoroborates.
| | Uses | P(t-Bu)3 Pd G2 (Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)] palladium(II), Pd/P(t-Bu)3) may be used as catalyst in the following studies:- Synthesis of sterically hindered biaryls (tetra-ortho-substituted), via cross-coupling reactions of aryl chlorides.
- Stille cross-couplings reactions of aryl chloride.
- Synthesis of chloropeptin I, via Stille cross-coupling reaction.
- Heck reaction.
- Negishi cross-coupling reactions.
| | General Description | P(t-Bu)3 Pd G2 (Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)] palladium(II)) is a second generation (G2) precatalyst containing a biphenyl-based ligand. Product participates in various palladium catalyzed cross-coupling reactions, C-C, C-N and C-O bond formation reactions, and Suzuki-Miyaura coupling reactions. It generates active Pd catalyst at room temperature in the presence of weak phosphate or carbonate bases. It has been proposed as an active catalyst for use in Stille reactions of aryl halides (bromides and chlorides). |
| Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II) Preparation Products And Raw materials |
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![Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II)](/img/1375325-71-5.jpg "Chloro[(tri-tert-butylphosphine)-2-(2-aMinobiphenyl)]palladiuM(II)")
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