ChemicalBook--->CAS DataBase List--->5779-93-1

5779-93-1

5779-93-1 Structure

5779-93-1 Structure
IdentificationMore
[Name]

2,3-Dimethylbenzaldehyde
[CAS]

5779-93-1
[Synonyms]

2,3-DIMETHYLBENZALDEHYDE
O-XYLENE-3-CARBOXALDEHYDE
2,3-Dimethylbenzaldehyd
Hemellitaldehyde
[EINECS(EC#)]

611-577-9
[Molecular Formula]

C9H10O
[MDL Number]

MFCD00798004
[Molecular Weight]

134.18
[MOL File]

5779-93-1.mol
Chemical PropertiesBack Directory
[Boiling point ]

86-88 °C10 mm Hg(lit.)
[density ]

1.029 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.553(lit.)
[Fp ]

215 °F
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Chloroform, Methanol
[form ]

Liquid
[color ]

Colorless to pale yellow
[CAS DataBase Reference]

5779-93-1(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Safety Statements ]

24/25
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

29122990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Sodium hydroxide-->Hydrochloric acid-->Ethyl acetate-->Methanol-->Acetic acid-->Magnesium sulfate-->Triethylamine-->Sodium bicarbonate-->Pyridine-->Ammonium chloride-->Formaldehyde-->Carbon tetrachloride-->Iodomethane-->N-Bromosuccinimide-->Sodium bisulfite-->Dimethylamine-->Benzoyl peroxide-->Bromoethane-->Sodium acetate trihydrate-->Hexamethylenetetramine-->Sodium amide-->2-Methylbenzyl chloride-->1,2,3-Trimethylbenzene
Hazard InformationBack Directory
[Chemical Properties]

Clear Colorless Oil
[Uses]

The major component of the umbel rays oil.
[Synthesis]

2,3-Dimethylbromobenzene

576-23-8

N,N-Dimethylformamide

68-12-2

2,3-Dimethylbenzaldehyde

5779-93-1

Magnesium chips (26.4 g, 1.1 mol) and tetrahydrofuran (160 mL) were added to the reaction flask under nitrogen protection, and a mixture of 1-bromo-2,3-dimethylbenzene (18.5 g, 0.1 mol) and tetrahydrofuran (100 mL) was added dropwise with stirring at room temperature to initiate the reaction. Subsequently, a mixture of 1-bromo-2,3-dimethylbenzene (166.5 g, 0.9 mol) and tetrahydrofuran (1000 mL) was added dropwise to the reaction system. After the dropwise addition, the reaction mixture was refluxed for 1 hour. The resulting Grignard reagent was cooled in an ice bath and a mixture of N,N-dimethylformamide (73 g, 1.0 mol) and tetrahydrofuran (300 mL) was added dropwise slowly, controlling the reaction temperature to not exceed 20 °C. The reaction temperature was then increased by 1 h at room temperature. After the dropwise addition was completed, the reaction was continued to be stirred for 2 hours at room temperature. At the end of the reaction, the reaction was quenched by the addition of saturated aqueous ammonium chloride solution (1000 mL) and left to stratify. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The organic phases were combined, washed with saturated saline (500 mL) and left to stratify. The organic phase was dried with anhydrous sodium sulfate (50 g), filtered and concentrated to dryness under reduced pressure to give 2,3-dimethylbenzaldehyde in 96% yield and 96.2% purity.

[References]

[1] Patent: CN105503551, 2016, A. Location in patent: Paragraph 0012; 00013
Spectrum DetailBack Directory
[Spectrum Detail]

2,3-Dimethylbenzaldehyde(5779-93-1)1HNMR
2,3-Dimethylbenzaldehyde(5779-93-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

5779-93-1(sigmaaldrich)
[TCI AMERICA]

2,3-Dimethylbenzaldehyde,>96.0%(GC)(5779-93-1)
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