Identification | More | [Name]
4-CHLORO-2-METHYLBENZONITRILE | [CAS]
50712-68-0 | [Synonyms]
2-METHYL-4-CHLOROBENZONITRILE 4-CHLORO-2-METHYLBENZONITRILE | [Molecular Formula]
C8H6ClN | [MDL Number]
MFCD00045603 | [Molecular Weight]
151.59 | [MOL File]
50712-68-0.mol |
Chemical Properties | Back Directory | [Melting point ]
57-61 °C (lit.) | [Boiling point ]
85-86°C/3mm | [density ]
1.19±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
powder | [color ]
beige crystilline | [InChI]
InChI=1S/C8H6ClN/c1-6-4-8(9)3-2-7(6)5-10/h2-4H,1H3 | [InChIKey]
ZZAJFWXXFZTTLH-UHFFFAOYSA-N | [SMILES]
C(#N)C1=CC=C(Cl)C=C1C | [CAS DataBase Reference]
50712-68-0(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
6.1 | [HazardClass ]
IRRITANT-HARMFUL | [HS Code ]
2926907090 |
Hazard Information | Back Directory | [Chemical Properties]
off-white crystalline | [Synthesis]
The general procedure for the synthesis of compounds (CAS:1117842-29-1) and 4-chloro-2-methylbenzonitrile from 2-cyanofuran and compounds (CAS:25961-46-0) was as follows: crude oxathiazolone compound (2.0 g, 8.8 mmol) was mixed with 2-furanonitrile (16 g, 170 mmol) in a microwave reactor under 190°C for 20 min. This reaction was repeated for 10 batches, and the reaction solution was combined and subjected to Kugelrohr distillation at 100 °C, 30 mbar to recover excess 2-furanonitrile (for use in the next microwave reaction). Subsequently, the residue was further distilled at 150 °C, 20 mbar to remove the nitrile by-products. 5.5 g of the residue was combined with 4.5 g of the residue obtained from another 10 microwave reactions and purified by column chromatography. The 4.5 g of product obtained (HPLC purity 85%) was dissolved in methanol (50 mL) and recrystallized to give pure 3-(4-chloro-2-methylphenyl)-5-(furan-2-yl)-1,2,4-thiadiazole as a light brown solid in 3.6 g yield (7.5% yield). Chemical formula: C13H9ClN2OS; Molecular weight: 278.7; HPLC-ESMS: retention time tR = 6.36 min, m/z 277.0 (M + 1); HPLC purity: > 95% (220 nm), 95% (270 nm). 1H-NMR (300 MHz, CDCl3): δ 8.06 (dd, J = 7.8 Hz, 1H), 7.62-7.63 (m, 1H), 7.22-7.31 (m, 3H), 6.61-6.63 (m, 1H), 2.66 (s, 3H). | [References]
[1] Patent: US2009/48311, 2009, A1. Location in patent: Page/Page column 42 |
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