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3-(1-methylethyl)-pyrazole

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3-(1-methylethyl)-pyrazole Basic information
Product Name:3-(1-methylethyl)-pyrazole
Synonyms:3-(1-Methylethyl)-1H-pyrazole;3-isopropyl-1H-pyrazole;1H-Pyrazole, 3-(1-methylethyl)-;5-isopropyl-1H-pyrazole(SALTDATA: FREE);5-Isopropyl-1H-pyrazole;3-(propan-2-yl)-1H-pyrazole;3(5)-isopropyl-1H-pyrazole;3-(1-methylethyl)-pyrazole
CAS:49633-25-2
MF:C6H10N2
MW:110.16
EINECS:
Product Categories:heterocyclic/Aliphatic series;Heterocycles
Mol File:49633-25-2.mol
3-(1-methylethyl)-pyrazole Structure
3-(1-methylethyl)-pyrazole Chemical Properties
Boiling point 115 °C(Press: 12 Torr)
density 0.991±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka14.32±0.10(Predicted)
AppearanceColorless to light yellow Liquid
InChIInChI=1S/C6H10N2/c1-5(2)6-3-4-7-8-6/h3-5H,1-2H3,(H,7,8)
InChIKeyZICRALLMHKILDG-UHFFFAOYSA-N
SMILESN1C=CC(C(C)C)=N1
CAS DataBase Reference49633-25-2(CAS DataBase Reference)
Safety Information
HazardClass IRRITANT
HS Code 2933199090
MSDS Information
3-(1-methylethyl)-pyrazole Usage And Synthesis
Synthesis
1-(Dimethylamino)-4-methyl-1-penten-3-one

5782-56-9

3-(1-methylethyl)-pyrazole

49633-25-2

Step 4: Preparation of 3-isopropyl-1H-pyrazole (88b). 1-(Dimethylamino)-4-methylpent-1-en-3-one (87) (6.6 g, 1 eq.) was slowly added dropwise to a stirred mixed solution of hydrazine monochloride (3.2 g, 1 eq.), sulfuric acid (1.13 mL) and water (6 mL). The reaction mixture was stirred at 68 °C for 2 hours. Upon completion of the reaction, the reaction mixture was neutralized with 1N NaOH solution and subsequently extracted with ether. The organic layers were combined, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure to afford the target product 3-isopropyl-1H-pyrazole (88b) as a beige solid in 94% yield.1H NMR (DMSO-d6, 400 MHz) δ: 1.17 (s, 3H), 1.19 (s, 3H), 2.87-2.93 (m, 1H), 5.99 ( s, 1H), 7.40 (s, 1H), 1.39-1.43 (t, J = 7.04 Hz, 3H), 4.08-4.13 (q, J = 7.04 Hz, 2H), 5.86 (d, J = 12.40 Hz, 1H), 7.90 (d, J = 12.40 Hz, 1H).

References[1] Patent: WO2009/14730, 2009, A1. Location in patent: Page/Page column 132
[2] Patent: US2004/63744, 2004, A1. Location in patent: Page/Page column 89
[3] Patent: WO2011/17389, 2011, A1. Location in patent: Page/Page column 152
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