5-Methyl-6-nitrobenzo[d][1,3]dioxole

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5-Methyl-6-nitrobenzo[d][1,3]dioxole Basic information
Product Name:5-Methyl-6-nitrobenzo[d][1,3]dioxole
Synonyms:5-Methyl-6-nitrobenzo[d][1,3]dioxole;1,3-Benzodioxole, 5-methyl-6-nitro-
CAS:32996-27-3
MF:C8H7NO4
MW:181.15
EINECS:
Product Categories:
Mol File:32996-27-3.mol
5-Methyl-6-nitrobenzo[d][1,3]dioxole Structure
5-Methyl-6-nitrobenzo[d][1,3]dioxole Chemical Properties
Melting point 102-104 °C
Boiling point 289.8±39.0 °C(Predicted)
density 1.407±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
AppearanceLight yellow to yellow Solid
Safety Information
HS Code 2932990090
MSDS Information
5-Methyl-6-nitrobenzo[d][1,3]dioxole Usage And Synthesis
Synthesis
5-METHYL-1,3-BENZODIOXOLE

7145-99-5

5-Methyl-6-nitrobenzo[d][1,3]dioxole

32996-27-3

Step A: 5-methyl-1,3-benzodioxole (8.00 g, 58.8 mmol) was dissolved in chloroform (160 mL) and stirred under ice bath cooling. 60% nitric acid (20 mL) was slowly added dropwise to the reaction system, and after dropping, stirring was continued for 30 minutes at room temperature. After completion of the reaction, the reaction mixture was diluted with dichloromethane, washed sequentially with water and saturated sodium bicarbonate solution, and dried over anhydrous potassium carbonate. The desiccant was removed by filtration and the filtrate was concentrated under reduced pressure to give a light yellow solid 5-methyl-6-nitrobenzo[d][1,3]dioxole (9.58 g, 90% yield).1H-NMR (300 MHz, CDCl3) δ: 2.55 (s, 3H), 6.08 (s, 2H), 6.70 (s, 1H), 7.50 (s, 1H).

References[1] Patent: US2012/196824, 2012, A1
[2] Patent: US2003/87842, 2003, A1
[3] Patent: US2004/77554, 2004, A1
[4] Yakugaku Zasshi, 1933, vol. 53, p. 73,83, 118; dtsch. Ref. S. 11, 22
[5] Chem. Zentralbl., 1933, vol. 104, # I, p. 3201,3203
5-Methyl-6-nitrobenzo[d][1,3]dioxole Preparation Products And Raw materials
Raw materials5-Methyl-1,3-benzodioxole-->Chloroform-->Nitric acid
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