Benzaldehyde → HCID 59338814, compound

HRID 12576Notes

Reaction equation

HRID 12576 reaction equation
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:9][O:10][C:11]([C:13](=[CH:34][CH:35]=[CH:36][C:37]1[CH:42]=[CH:41][C:40]([CH:43]([CH3:45])[CH3:44])=[CH:39][CH:38]=1)[N:14]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:12]>C(#N)C>[CH:43]([C:40]1[CH:39]=[CH:38][C:37]([C:36]2[CH:35]=[CH:34][C:13]([C:11]([O:10][CH3:9])=[O:12])=[N:14][C:1]=2[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:42][CH:41]=1)([CH3:44])[CH3:45]

Participants

4

Reactant 2

HCID 240BenzaldehydeHCID 722584753-Methoxycarbonyl-1,1,1-triphenyl-6-(4-isopropylphenyl)-2-aza-1lambda5-phosphahexa-1,3,5-triene2×

Product 1

HCID 59338814HCID 59338814, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Following General Procedure K, Benzaldehyde (0.48 g, 4.6 mmol) and 3-Methoxycarbonyl-1,1,1-triphenyl-6-(4-isopropylphenyl)-2-aza-1λ5-phosphahexa-1,3,5-triene (Compound 112, 2.3 g, 4.6 mmol) in dry acetonitrile (100 ml) were reacted to produce the title compound as a yellow solid.

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-a03d48d4ac1048bd95386f3dae143d76
Source dataset
uspto-grants-2010_06
Patent number
US07728014B2

Reaction notes

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