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364975

(Triphenylphosphine)copper hydride hexamer

90%

Synonym(s):

Cuprous hydride triphenylphosphine hexamer, Hydrido(triphenylphosphine)copper(I) hexamer, Stryker’s reagent, Triphenylphosphine–Copper(I) hydride Hexamer

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About This Item

Linear Formula:
[(C6H5)3PCuH]6
CAS Number:
33636-93-0
Molecular Weight:
1961.04
NACRES:
NA.22
PubChem Substance ID:
24862472
UNSPSC Code:
12352002
MDL number:
MFCD00221518
Assay:
90%
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Quality Segment

100

assay

90%

reaction suitability

reagent type: reductant

functional group

phosphine

SMILES string

[CuH].[CuH].[CuH].[CuH].[CuH].[CuH].c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6.c7ccc(cc7)P(c8ccccc8)c9ccccc9.c%10ccc(cc%10)P(c%11ccccc%11)c%12ccccc%12.c%13ccc(cc%13)P(c%14ccccc%14)c%15ccccc%15.c%16ccc(cc%16)P(c%17ccccc%17)c%18ccccc%18

InChI

1S/6C18H15P.6Cu.6H/c6*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;;;;;;;;;;/h6*1-15H;;;;;;;;;;;;

InChI key

PYHLOCIDGQNZFY-UHFFFAOYSA-N

General description

Triphenylgermanium hydride is a hydrogen donor.

Application

Some useful synthetic applications of (Triphenylphosphine)copperhydride hexamer include stoichiometric and catalytic hydrogenations, chemoselective conjugate reductions, as well as regiospecific and stereoselectiveconjugate hydride reductions.
Catalyst for:
  • Conjugate reduction of ortho-substituted cinnamic esters to form copper enolates
  • Chemoselective preparation of alcohols via hydrogenation of aldehydes
  • 1,2-addition/transmetalation reactions
  • Synthesis of monomer for preparation of phosphorus- and silicon-containing epoxy resins
  • Hydrosilylation reactions
  • Chiral hydrogenation reactions
  • Hydrostannation of activated alkynes

pictograms

Flame
GHS02

signalword

Warning

hcodes

H228

Hazard Classifications

Flam. Sol. 2

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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