Diphenylacetonitril

Diphenylacetonitrile

HCID 6837CAS 86-29-3

Grundinformationen

Standard-SMILES
N#CC(c1ccccc1)c1ccccc1
InChIKey
NEBPTMCRLHKPOB-UHFFFAOYSA-N
Summenformel
C14H11N
Durchschnittliche Molmasse
193,24 g/mol
Monoisotopische Masse
193,08914936

Namen und Bezeichner

Bevorzugter Name
Diphenylacetonitrile
IUPAC
2,2-diphenylacetonitrile
Lokaler Name
Diphenylacetonitril
Englischer Name
Diphenylacetonitrile
Summenformel
C14H11N
Molmasse
193.25

Namen und Synonyme

DIPHENYLACETONITRILE86-29-3DipanDiphenatrileBenzhydrylcyanideBenzyhydrylcyanidebenzhydryl cyanideDiphenylmethylcyanideDiphenylmethyl cyanideDifenylacetonitrilAcetonitrile, diphenyl-USAF KF-13
Weitere Namen anzeigen
2,2-diphenylacetonitrileDPANdibenzylcyanide-CyanodiphenylmethaneBenzeneacetonitrile, α-phenyl-
alpha-PhenylbenzeneacetonitrileDiphenyl-alpha-cyanomethanealpha-PhenylphenylacetonitrileBenzeneacetonitrile, alpha-phenyl-Caswell No. 396alpha-Phenylbenzylcyanidealpha-CyanodiphenylmethaneDifenylacetonitril [Czech]

Datenbank-Bezeichner

CAS
86-29-3
PubChem CID
6837
DTXSID
DTXSID4020539
ChEMBL
CHEMBL3185477
UNII
QK4W106TKU
EC Number
201-662-5
Nikkaji
J4.937I

Eigenschaften

Berechnete Struktureigenschaften

XLogP
3,2
Polarare Oberfläche (TPSA)
23,8 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
1
Frei drehbare Bindungen
2
Schwere Atome
15

Physikochemische Eigenschaften

Schmelzpunkt
71 · 71-73 °C (lit.)
Siedepunkt
181 °C/12 · 181 °C/12 mmHg (lit.)
Dichte
1.1061 · 1.1061 (rough estimate)
Dampfdruck
21.3 hPa · 21.3 hPa (190 °C)
Brechungsindex
1.585 · 1.5850 (estimate)
Flammpunkt
120 °C · 120 °C

Sicherheit und Regulatorisches

Sicherheitsdaten

wgk
2
tsca
TSCA listed
hs_code
29269095
RTECS-Nr.
AL9800000
risk_code
36/37/38
Toxizität
LD50 orally in Rabbit: 3500 mg/kg

Chemie und Industrie

Anwendungen · 1 Eintrag

VerwendenMathadone (M225865) impurity. Used in synthesis of methadone, antispasmodics and other pharmaceuticals.Diphenylacetonitrile is used to synthesize isocyanate, which is further prepared into UV paint, PU paint, transparent elastomer and adhesive, etc. In addition, it is also used in polyamide and epoxy resin industries.

Darstellung · 2 Einträge

synthetischeIn a 100 mL, nitrogen-flushed pear flask was added indium(III) bromide (2.0 mmol, 10 mol %) in CH2Cl2 (40 mL) to give a white suspension. To this at room temperature was added trimethylsilyl cyanide (40 mmol, 2.0 equiv.), followed by dropwise addition of alcohol (20 mmol, 1.0 equiv.) to give a moderate exothermic reaction. The mixture slowly turned clear, and TLC showed mostly the desire product. Saturated NaHCO3 was added and the mixture was concentrated in vacuo to remove the volatiles. The residue was partitioned between saturated NaHCO3 and ethyl acetate, and the aqueous layer was extracted one more time with ethyl acetate. Combined organic layers were dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography on silica gel (5% ethyl acetate/hexanes) to give the desired Diphenylacetonitrile.

synthetischeDiphenylacetonitrile can be prepared in good yield by the dehydration of the amide of diphenyl acetic acid with phosphorous oxychloride. Diphenylacetonitrile undergoes anhydrous condensation with ethyl-4-bromo-butyrate. This is followed by its hydrolysis in alkaline medium that is used in the quantitative determination of 3-cyano-3,3-diphenylpropionic acid.

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