ChemicalBook--->CAS DataBase List--->59997-51-2

59997-51-2

59997-51-2 Structure

59997-51-2 Structure
IdentificationMore
[Name]

Pivaloylacetonitrile
[CAS]

59997-51-2
[Synonyms]

1-CYANO-3,3-DIMETHYL-2-BUTANONE
4,4-DIMETHYL-3-OXO-N-VALERONITRILE
4,4-DIMETHYL-3-OXOPENTANENITRILE
4,4-dimethyl-3-oxovaleronitrile
CYANOPINACOLONE
PIVALOYLACETONITRILE
TIMTEC-BB SBB008437
TRIMETHYLACETYLACETONITRILE
4,4-dimethyl-3-oxo-pentanenitril
Pentanenitrile, 4,4-dimethyl-3-oxo-
1-Cyanopinacolone
Pivaloyl Acetonitrile 99%min
4,4-DIMETHYL-3-OXOVALERONITRILE(PIVALOYLACETONITRILE)
4,4,-Dimethyl-3-Ox-Valeronitrile(Pivaloylacetonitrile)
Trimethylacetylacetonitrile, 98+%
Trimethylacetylacetonitrile,99%
4,4-DIMETHYL-3-OXOPENTANENITRILE(PIVALOYLACETONITRILE)
PIVALOYLACETONITRILE (4,4-DIMETHYL-3-OXOPENTANENITRILE) (1-CYANOPINACOLONE)
Valeronitrile, 4,4-dimethyl-3-oxo
3-Oxo-4,4-dimethylpentanenitrile
[EINECS(EC#)]

262-017-1
[Molecular Formula]

C7H11NO
[MDL Number]

MFCD00010208
[Molecular Weight]

125.17
[MOL File]

59997-51-2.mol
Chemical PropertiesBack Directory
[Appearance]

white to cream crystals or crystalline powder
[Melting point ]

66-69 °C(lit.)
[Boiling point ]

125-126 °C22 mm Hg(lit.)
[density ]

1.0459 (rough estimate)
[refractive index ]

1.4693 (estimate)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

Crystals or Crystalline Powder
[pka]

10.25±0.10(Predicted)
[color ]

White to cream
[Water Solubility ]

Insoluble in water.
[BRN ]

1746674
[InChI]

InChI=1S/C7H11NO/c1-7(2,3)6(9)4-5-8/h4H2,1-3H3
[InChIKey]

MXZMACXOMZKYHJ-UHFFFAOYSA-N
[SMILES]

C(#N)CC(=O)C(C)(C)C
[CAS DataBase Reference]

59997-51-2(CAS DataBase Reference)
[NIST Chemistry Reference]

4,4-Dimethyl-3-oxopentanenitrile(59997-51-2)
[EPA Substance Registry System]

Pentanenitrile, 4,4-dimethyl-3-oxo- (59997-51-2)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P264-P270-P301+P310a-P321-P405-P501a-P301+P310
[Hazard Codes ]

T
[Risk Statements ]

R25:Toxic if swallowed.
[Safety Statements ]

S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 3439 6.1/PG 3
[WGK Germany ]

3
[RTECS ]

SA2991000
[F ]

8
[TSCA ]

Yes
[REACH Registrations]

Active
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29269090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Isoxazole, 3,5-bis(1,1-dimethylethyl)--->N-Methoxy-N,2,2-trimethylpropanamide-->1-Bromopinacolone-->Ethyl trimethylacetate-->Sodium cyanide-->Methyl trimethylacetate-->1-Chloropinacolone-->1,4-Dioxane-->Acetonitrile-->Pinacolone
[Preparation Products]

3-tert-Butylisoxazol-5-amine-->5-Amino-3-tert-butyl-1-methylpyrazole
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

4,4-Dimethyl-3-oxovaleronitrile(59997-51-2).msds
Hazard InformationBack Directory
[Chemical Properties]

white to cream crystals or crystalline powder
[Uses]

Trimethylacetylacetonitrile is a useful intermediate. 4,4-Dimethyl-3-oxopentanenitrile has been used in the preparation of 4,4-dimethyl-3-oxo-2-benzylpentanenitrile, 4,4-dimethyl-3-oxo-2-(4-hydroxybenzyl)pentanenitrile, 4,4-dimethyl-3-oxo-2-(4-methoxybenzyl)pentanenitrile, 4,4-dimethyl-3-oxo-2-(4-fluorobenzyl)pentanenitrile, 4,4-dimethyl-3-oxo-2-(3,4-methylenedioxybenzyl)pentanenitrile, 1-(5-tert-butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-phenylurea.
[Synthesis]

Methyl trimethylacetate

598-98-1

Acetonitrile

75-05-8

Pivaloylacetonitrile

59997-51-2

1. NaH (50% in paraffin oil, 1.2 eq., 4.6 g) was added to 1,4-dioxane (120 ml) and stirred for several minutes to disperse the mixture. 2. Acetonitrile (1.2 eq., 4.2 g) was slowly added dropwise to the above mixture over a period of 15 minutes and stirring was continued for 30 minutes after completion of the addition. 3. Methyl pivalate (1 eq., 10 g) was added slowly and dropwise to the reaction system over 15 minutes, after which the reaction mixture was heated to reflux for 3 hours. 4. After completion of the reaction, the reaction mixture was poured into ice water (200 g) and the pH was adjusted to 4.5 with acid. 5. The aqueous phase was extracted several times with dichloromethane (12 x 250 ml) and the organic phase was combined. 6. The combined organic phases were dried with anhydrous sodium sulfate, filtered and concentrated. 7. The concentrate was recrystallized with hexane (100 ml) to give the brown solid product 4,4-dimethyl-3-oxopentanenitrile (5 g, 51% yield).

[References]

[1] Tetrahedron, 1993, vol. 49, # 23, p. 5091 - 5098
[2] Journal of the Chemical Society, Chemical Communications, 1992, # 1, p. 50 - 51
[3] Patent: WO2010/127855, 2010, A1. Location in patent: Page/Page column 95
[4] Patent: WO2010/127856, 2010, A1. Location in patent: Page/Page column 78
[5] Patent: US2012/46301, 2012, A1. Location in patent: Page/Page column 28; 29
Spectrum DetailBack Directory
[Spectrum Detail]

Pivaloylacetonitrile(59997-51-2)MS
Pivaloylacetonitrile(59997-51-2)1HNMR
Pivaloylacetonitrile(59997-51-2)13CNMR
Pivaloylacetonitrile(59997-51-2)IR1
Pivaloylacetonitrile(59997-51-2)IR2
Pivaloylacetonitrile(59997-51-2)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Pivaloylacetonitrile, 97%(59997-51-2)
[Alfa Aesar]

Trimethylacetylacetonitrile, 99%(59997-51-2)
[Sigma Aldrich]

59997-51-2(sigmaaldrich)
[TCI AMERICA]

Pivaloylacetonitrile,>98.0%(GC)(59997-51-2)
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