DIPAMP
Names
Preferred IUPAC name
(Ethane-1,2-diyl)bis[(2-methoxyphenyl)(phenyl)phosphane]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.203.286
UNII
  • InChI=1S/C28H28O2P2/c1-29-25-17-9-11-19-27(25)31(23-13-5-3-6-14-23)21-22-32(24-15-7-4-8-16-24)28-20-12-10-18-26(28)30-2/h3-20H,21-22H2,1-2H3
    Key: QKZWXPLBVCKXNQ-UHFFFAOYSA-N
  • (R,R): InChI=1S/C28H28O2P2/c1-29-25-17-9-11-19-27(25)31(23-13-5-3-6-14-23)21-22-32(24-15-7-4-8-16-24)28-20-12-10-18-26(28)30-2/h3-20H,21-22H2,1-2H3/t31-,32-/m1/s1
    Key: QKZWXPLBVCKXNQ-ROJLCIKYSA-N
  • (S,S): InChI=1S/C28H28O2P2/c1-29-25-17-9-11-19-27(25)31(23-13-5-3-6-14-23)21-22-32(24-15-7-4-8-16-24)28-20-12-10-18-26(28)30-2/h3-20H,21-22H2,1-2H3/t31-,32-/m0/s1
    Key: QKZWXPLBVCKXNQ-ACHIHNKUSA-N
  • (R,S): InChI=1S/C28H28O2P2/c1-29-25-17-9-11-19-27(25)31(23-13-5-3-6-14-23)21-22-32(24-15-7-4-8-16-24)28-20-12-10-18-26(28)30-2/h3-20H,21-22H2,1-2H3/t31-,32+
    Key: QKZWXPLBVCKXNQ-MEKGRNQZSA-N
  • COc1ccccc1P(CCP(c2ccccc2)c3ccccc3OC)c4ccccc4
  • (R,R): COc1ccccc1[P@](CC[P@](c2ccccc2)c3ccccc3OC)c4ccccc4
  • (S,S): COc1ccccc1[P@@](CC[P@@](c2ccccc2)c3ccccc3OC)c4ccccc4
  • (R,S): O(c1ccccc1[P@@](c2ccccc2)CC[P@@](c3ccccc3)c4ccccc4OC)C
Properties
C28H28O2P2
Molar mass 458.478 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

DIPAMP is an organophosphorus compound that is used as a ligand in homogeneous catalysis. It is a white solid that dissolves in organic solvents. Work on this compound by W. S. Knowles was recognized with the Nobel Prize in Chemistry.[1] DIPAMP was the basis for one of the first industrial scale asymmetric hydrogenation, the synthesis of the drug L-DOPA.[2]

Synthesis of L-DOPA via hydrogenation with the C2-symmetric diphosphine DIPAMP.

DIPAMP is a C2-symmetric diphosphine. Each phosphorus centre, which is pyramidal, bears three different substituents - anisyl, phenyl, and the ethylene group. The ligand therefore exists as the enantiomeric (R,R) and (S,S) pair, as well as the achiral meso isomer.

DIPAMP was originally prepared by an oxidative coupling, starting from anisyl(phenyl)(methyl)phosphine.

Structure of [Rh(DIPAMP)(cod)]+ by X-ray crystallography.[3]

References

  1. ↑ Knowles, William S. (2002). "Asymmetric Hydrogenations (Nobel Lecture) Copyright© The Nobel Foundation 2002. We thank the Nobel Foundation, Stockholm, for permission to print this lecture". Angewandte Chemie International Edition. 41 (12): 1998. doi:10.1002/1521-3773(20020617)41:12<1998::AID-ANIE1998>3.0.CO;2-8.
  2. ↑ Vineyard, B. D.; Knowles, W. S.; Sabacky, M. J.; Bachman, G. L.; Weinkauff, D. J. (1977). "Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst". Journal of the American Chemical Society. 99 (18): 5946–5952. doi:10.1021/ja00460a018.
  3. ↑ H.-J.Drexler; Songlin Zhang; Ailing Sun; A. Spannenberg; A. Arrieta; A. Preetz; D. Heller (2004). "Cationic Rh-bisphosphine-diolefin complexes as precatalysts for enantioselective catalysis––what information do single crystal structures contain regarding product chirality?". Tetrahedron: Asymmetry. 15 (14): 2139–50. doi:10.1016/j.tetasy.2004.06.036.
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