ChemicalBook--->CAS DataBase List--->25263-44-9

25263-44-9

25263-44-9 Structure

25263-44-9 Structure
IdentificationBack Directory
[Name]

M-HYDROXY BENZYL CYANIDE
[CAS]

25263-44-9
[Synonyms]

M-HYDROXY BENZYL CYANIDE
3-hydroxyphenyacetonitrile
3-HYDROXYPHENYLACETONITRILE
M-HYDROXYPHENYLACETONITRILE
3-Hydroxy-Benzeneacetonitrile
Benzeneacetonitrile, 3-hydroxy-
2-(3-hydroxyphenyl)acetonitrile
M-HYDROXY BENZYL CYANIDE(3-HYDROXYPHENYL)-ACETONITRILE
[Molecular Formula]

C8H7NO
[MDL Number]

MFCD03265300
[MOL File]

25263-44-9.mol
[Molecular Weight]

133.15
Chemical PropertiesBack Directory
[Melting point ]

53 °C
[Boiling point ]

305.5±17.0 °C(Predicted)
[density ]

1.167±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

9.51±0.10(Predicted)
[color ]

White to Orange to Green
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2926.90.5050
Hazard InformationBack Directory
[Uses]

2-(3-Hydroxyphenyl)acetonitrile is used in preparation of Pyrrolidine Sulfonamide compounds as TRPV4 antagonists.
[Synthesis]

(3-Methoxyphenyl)acetonitrile

19924-43-7

M-HYDROXY BENZYL CYANIDE

25263-44-9

Step 1: Dissolve 2-(3-methoxyphenyl)acetonitrile (2 g, 13.59 mmol) in 13 mL of anhydrous dichloromethane under nitrogen protection and cool to 0°C. A 1 M solution of boron tribromide in dichloromethane (28.54 mL, 28.54 mmol) was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was stirred at room temperature for 20 hours. After completion of the reaction, the mixture was poured into ice water and extracted three times with dichloromethane. The organic phases were combined, washed with brine and dried over anhydrous sodium sulfate. After concentration under reduced pressure, the crude product was purified by silica gel column chromatography using petroleum ether/ethyl acetate (80/20) as eluent to give 1.28 g (71% yield) of 2-(3-hydroxyphenyl)acetonitrile.

[References]

[1] Patent: US2006/142553, 2006, A1. Location in patent: Page/Page column 11 - 12
[2] Patent: WO2008/46598, 2008, A1. Location in patent: Page/Page column 57
[3] Patent: WO2013/651, 2013, A1. Location in patent: Page/Page column 35; 55
[4] Patent: US2014/88074, 2014, A1. Location in patent: Paragraph 0286; 0287; 0524; 0525
[5] Patent: US6180627, 2001, B2
Spectrum DetailBack Directory
[Spectrum Detail]

M-HYDROXY BENZYL CYANIDE(25263-44-9)1HNMR
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