Home >Pharmaceutical > 2,3-DIMETHYL-2,3-DINITROBUTANE
- Chemical Name: 2,3-DIMETHYL-2,3-DINITROBUTANE
- CAS No.: 3964-18-9
Cost-effective and customizable 2,3-DIMETHYL-2,3-DINITROBUTANE 3964-18-9 factory
- Molecular Formula: C6H12N2O4
- Molecular Weight: 176.172
- Appearance/Colour: white to off-white crystal or crystalline powder
- Vapor Pressure: 0.117mmHg at 25°C
- Melting Point: 214-215 °C (dec.)(lit.)
- Refractive Index: 1.458
- Boiling Point: 219.8 °C at 760 mmHg
- Flash Point: 80.2 °C
- PSA: 91.64000
- Density: 1.15 g/cm3
- LogP: 2.14340
2,3-DIMETHYL-2,3-DINITROBUTANE(Cas 3964-18-9) Usage
|
Synthesis Reference(s) |
Journal of the American Chemical Society, 96, p. 2580, 1974 DOI: 10.1021/ja00815a043The Journal of Organic Chemistry, 35, p. 295, 1970 |
|
Synthesis |
The synthesis of 2,3-dimethyl-2,3-dinitrobutane is as follows:Add 4.5 g (0.05 mol) of 2-nitropropane and 9 mL of a 6 mol/L sodium hydroxide solution to a 100 mL three-necked flask. The reaction was stirred magnetically for 0.5 h in an ice-water bath, and 4 g (0.025 mol) of liquid bromine was added dropwise to the flask using a constant pressure dropping funnel. After the dropwise addition was completed, 15 mL of absolute ethanol was added to thereto, and stirring was continued in an ice bath for 0.5 h. Then the ice bath was removed, the temperature was raised to 90℃, and the reaction was refluxed for 2 hours to stop the reaction. After the reaction liquid was naturally cooled to room temperature, a large amount of white solid precipitated, filtered, washed several times with absolute ethanol and distilled water, and dried under vacuum to obtain 40.13 g of white flake crystals. The yield was 91.2%. |
InChI:InChI=1/C6H12N2O4/c1-5(2,7(9)10)6(3,4)8(11)12/h1-4H3
3964-18-9 Relevant articles
Ion Pairing and Solvent Effects in the Reactivity of Anions toward Free Radicals
Russell, Glen A.,Ros, Francisco,Mudryk, Boguslaw
, p. 7601 - 7603 (1980)
-
A NOVEL SRN1 SUBSTITUTION: THE REACTION BETWEEN THE ANION OF 2-NITROPROPANE AND 3-BROMO-1-NITROCYCLOHEX-1-ENE
Bowman, W. Russel,Brown, David S.,Leung, Christina T. W.,Stutchbury, Andrew P.
, p. 539 - 540 (1985)
X-ray crystallography has been used to d...
-
Astle,M.J.,Donat,F.J.
, p. 507 - 511 (1960)
-
Polynitro-Substituted Strained-Ring Compounds. Synthesis, Mechanism of Formation, and Structure of trans-Dinitrocyclopropanes
Wade, Peter A.,Dailey, William P.,Carroll, Patrick J.
, p. 5452 - 5456 (1987)
1,2-Dinitrocyclopropane, 1,2-dimethyl-1,...
Consecutive SRN1 and ERC1 Reactions in 5-Nitroisoquinolines
Vanelle, Patrice,Rathelot, Pascal,Maldonado, Jose,Crozet, Michel P.
, p. 8385 - 8388 (1994)
The reaction of 1-(dichloromethyl)-5-nit...
Efficient synthesis of a peculiar vicinal diamine semiochemical from streptomyces natalensis
Morin, Jesse B.,Sello, Jason K.
, p. 3522 - 3524 (2010)
(Equation Presented). The pimaricin-indu...
-
Bolsman,T.A.B.M.,de Boer,T.J.
, p. 1019 - 1023 (1975)
-
Alkali metal ion triggered conductive and stimuli-responsive metallogels
Chen, Shaorui,Li, Xiaoyuan,Yu, Xudong
, (2020/09/22)
A novel gelator NDH containing naphthali...
Nitroxide free radical, and preparation method and application thereof
-
Paragraph 0034-0035; 0044-0045, (2020/03/02)
The invention relates to a nitroxide fre...
Revisiting the Ullman's Radical Chemistry for Phthalocyanine Derivatives
Fidan, Ismail,Luneau, Dominique,Ahsen, Vefa,Hirel, Catherine
supporting information, p. 5359 - 5365 (2018/02/09)
Phthalocyanine derivatives do not cease ...
Combination of PhI(OAc)2 and 2-Nitropropane as the Source of Methyl Radical in Room-Temperature Metal-Free Oxidative Decarboxylation/Cyclization: Construction of 6-Methyl Phenanthridines and 1-Methyl Isoquinolines
Lu, Shi-Chao,Li, Hong-Shuang,Gong, Ya-Ling,Zhang, Shi-Peng,Zhang, Ji-Guo,Xu, Shu
, p. 15415 - 15425 (2019/01/03)
A room-temperature metal-free method for...
3964-18-9 Process route
-
-
79-46-9
2-nitropropane
-
-
66134-95-0
pyridyl-4-thiolate sodium salt
-
-
2645-22-9
dipyridin-4-yl disulfide
-
-
3964-18-9
2,3-dimethyl-2,3-dinitrobutane
-
-
1-methyl-1-nitroethyl 4-pyridyl sulphide
| Conditions | Yield |
|---|---|
|
With
sodium hydroxide; potassium hexacyanoferrate(III);
In
diethyl ether;
at 0 - 10 ℃;
for 1h;
|
22%
2% 14% |
-
-
595-49-3
2,2-dinitropropane
-
-
66134-95-0
pyridyl-4-thiolate sodium salt
-
-
2645-22-9
dipyridin-4-yl disulfide
-
-
3964-18-9
2,3-dimethyl-2,3-dinitrobutane
-
-
1-methyl-1-nitroethyl 4-pyridyl sulphide
| Conditions | Yield |
|---|---|
|
In
N,N,N,N,N,N-hexamethylphosphoric triamide;
for 20h;
|
4%
3% |
3964-18-9 Upstream products
-
67-56-1
methanol
-
38590-81-7
2-iodo-2-nitropropane
-
563-79-1
2,3-Dimethyl-2-butene
-
600-24-8
2-nitrobutane
3964-18-9 Downstream products
-
20485-44-3
2,3-dimethyl-2,3-diaminobutane
-
75-31-0
isopropylamine
-
14384-45-3
N,N'-dihydroxy-2,3-dimethylbutane-2,3-diamine
-
563-79-1
2,3-Dimethyl-2-butene