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Merck
CN

96004

JohnPhos

purum, ≥97.0% (GC)

Synonym(s):

(2-Biphenyl)di-tert-butylphosphine, (2-Biphenylyl)di-tert-butylphosphine, 2-(Di-tert-butylphosphino)biphenyl

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About This Item

Linear Formula:
C6H5C6H4P[C(CH3)3]2
CAS Number:
Molecular Weight:
298.40
PubChem Substance ID:
UNSPSC Code:
12350000
Beilstein/REAXYS Number:
8322131
MDL number:
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grade

purum

assay

≥97.0% (GC)

mp

86-88 °C (lit.)

Application

Ligand utilized in amination of aryl halides and aryl triflates.

Catalyst for:
  • Decarboxylative cross-coupling of dialkoxybenzoic acids with diaryl disulfides or diaryl diselenides
  • Stereoselective preparation of imidazolidinones via intramolecular hydroamination of N-allylic-N-arylureas
  • Regioselective arylation of olefins with aryl chlorides
  • Cross-coupling reaction for the synthesis of polyunsaturated macrolactones
  • Regioselective O-alkylation reactions
  • Sonogashira-type cross coupling

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Optimal ligand for a novel amination reaction (Buchwald reaction)

Regulatory Information

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J P Wolfe et al.
The Journal of organic chemistry, 65(4), 1158-1174 (2000-05-18)
Palladium complexes supported by (o-biphenyl)P(t-Bu)(2) (3) or (o-biphenyl)PCy(2) (4) are efficient catalysts for the catalytic amination of a wide variety of aryl halides and triflates. Use of ligand 3 allows for the room-temperature catalytic amination of many aryl chloride, bromide

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