4-(Hydroxy(phenyl)methyl)benzonitrile

Base Information

• Chemical Name: 4-(Hydroxy(phenyl)methyl)benzonitrile
• CAS No.: 13391-47-4
• Molecular Formula: C14H11 N O
• Molecular Weight: 209.247
• DSSTox Substance ID: DTXSID60446829
• Nikkaji Number: J465.363G
• Mol file: 13391-47-4.mol

Synonyms:13391-47-4;4-(HYDROXY(PHENYL)METHYL)BENZONITRILE;4-[HYDROXY(PHENYL)METHYL]BENZONITRILE;4-cyanobenzhydrol;4-Cyanobenzhydryl alcohol;SCHEMBL5664054;DTXSID60446829;FT-0725872

Chemical Property of 4-(Hydroxy(phenyl)methyl)benzonitrile

Chemical Property:

• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 209.084063974
• Heavy Atom Count: 16
• Complexity: 253

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(C2=CC=C(C=C2)C#N)O

Technology Process of 4-(Hydroxy(phenyl)methyl)benzonitrile

There total 24 articles about 4-(Hydroxy(phenyl)methyl)benzonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

terephthalonitrile (623-26-7) + benzaldehyde (100-52-7) → 4-cyanobenzhydrol (13391-47-4)

Guidance literature:

With pentanal; tetrabutylammonium acetate; In dimethyl sulfoxide; at 50 ℃; for 6h; Reagent/catalyst; Solvent; Electrochemical reaction;

DOI:10.1002/anie.202015230

Reference yield: 98.0%

4-cyanobenzaldehyde (105-07-7) + phenylboronic acid (98-80-6) → 4-cyanobenzhydrol (13391-47-4)

Guidance literature:

With palladium diacetate; caesium carbonate; triphenylphosphine; In chloroform; toluene; at 60 ℃; for 24h;

DOI:10.1021/ol051501y

Reference yield: 95.9%

potassium 4-methyl-1-phenyl-2,6,7-trioxa-1-borabicyclo-[2.2.2]octan-1-uide + 4-cyanobenzaldehyde (105-07-7) → 4-cyanobenzhydrol (13391-47-4)

Guidance literature:

With tri-1-napthylphosphine; palladium dichloride; In 1,4-dioxane; at 55 ℃; for 22h; Reagent/catalyst; Solvent;

upstream raw materials:

p-cyanobenzophenone

4-Cyanochlorobenzene

benzaldehyde

4-bromobenzenecarbonitrile

Downstream raw materials:

4-Cyan-benzhydrylchlorid

4-benzylbenzonitrile

1-(bis(4-iodophenyl)methyl)-1H-1,2,4-triazole

p-cyanobenzophenone