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Chemical Structure| 4984-85-4 Chemical Structure| 4984-85-4

Structure of Propioin
CAS No.: 4984-85-4

Chemical Structure| 4984-85-4

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Product Details of [ 4984-85-4 ]

CAS No. :4984-85-4
Formula : C6H12O2
M.W : 116.16
SMILES Code : OC(C(CC)=O)CC
English Name :4-Hydroxyhexan-3-one
MDL No. :MFCD00043572
InChI Key :SKCYVGUCBRYGTE-UHFFFAOYSA-N
Pubchem ID :95609

Safety of [ 4984-85-4 ]

Application In Synthesis of [ 4984-85-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 4984-85-4 ]

[ 4984-85-4 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 4984-85-4 ]
  • [ 4437-51-8 ]
YieldReaction ConditionsOperation in experiment
96.2% With water; ozone; acetic acid at 5℃; Green chemistry; 1-3 Embodiment 1 Embodiment 1 A step of 4-hydroxy-3-hexanone oxidation in a synthesis method of 3,4-hexanedione in the invention: first, 116.2 g of 4-hydroxy-3-hexanone (1 mol) and 41 g of water (2.5 mol) are added into a 500 mL three-necked flask for mixing, and then 1.5 g of acetic acid (0.025 mol) used as a cocatalyst is added into the three-necked flask; the three-necked flask is placed in a water bath pot for mixing and stirring by keeping at 5° C.; ozone is introduced into a mixture to carry out an oxidation reaction, a flow rate of the ozone is maintained at 0.3 L/min, and gas chromatography is used for tracking a reaction progress; after the reaction is completed, sodium bisulfite is added into a reaction system to remove ozone remaining in a solution (the ozone remaining in the solution is removed, and otherwise, residual ozone can continue to react to produce by-products during heating in a subsequent distillation process); finally distillation under reduced pressure for separation is carried out to obtain the finished product (3,4-hexanedione). With calculation of 4-hydroxy-3-hexanone, the yield of 3,4-hexanedione is 96.2% in the whole process. Products obtained in the embodiment 1 include: 1H NMR (400 MHz, CDCl3): δ 2.78 (4H, q, 2-CH2-); 1.11 (6H, t, 2-CH3).
86% With sodium bromide In dichloromethane; water Ambient temperature; anodic oxidation;
82% With pyridine; N-Bromosuccinimide In tetrachloromethane for 1.5h;
With selenium(IV) oxide
With copper diacetate; acetic acid
With water; iron(III) chloride
With nitric acid
With aluminum oxide; pumice stone at 320℃;
With Na<Sb(OAc)6> In 1,4-dioxane Heating;
With hydroxide at 22.85℃; Photolysis;
20 %Chromat. With oxygen; calcium oxide at 130℃; for 3h;

  • 2
  • [ 4984-85-4 ]
  • [ 760-02-1 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; <i>N</i>,<i>N</i>-dimethyl-aniline
With pyridine; thionyl chloride
  • 5
  • [ 4984-85-4 ]
  • [ 57-13-6 ]
  • [ 71624-06-1 ]
YieldReaction ConditionsOperation in experiment
75% In benzene for 4h; Heating;
54% for 0.0833333h; Irradiation;
With acetic acid
In ethanol Reflux; General procedure for the synthesis of 4,5-bis/disubstituted 1H-imidazol-2(3H)-ones (I1-15) General procedure: The compound from step one, 2-hydroxy-1,2-disubstituted ethanone E1-15 (0.01 mol) and urea (0.01 mol) were mixed in ethanol and refluxed for 3-4 h. Then, the reaction mixture was cooled, solid product was isolated by filtration and recrystallized from ethanol. The purity of the compound was established by thin-layer chromatography using toluene and cyclohexane (7:3) as a mobile phase.

  • 6
  • [ 4437-51-8 ]
  • [ 4984-85-4 ]
YieldReaction ConditionsOperation in experiment
Irradiation;
With tripotassium phosphate tribasic; Thauera aromatica alcohol dehydrogenase; nicotinamide adenine dinucleotide In aq. buffer Enzymatic reaction;
  • 7
  • [ 6838-59-1 ]
  • [ 4984-85-4 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride In diethyl ether Heating;
  • 8
  • [ 4984-85-4 ]
  • [ 105961-54-4 ]
YieldReaction ConditionsOperation in experiment
70% With sulfur tetrafluoride In diethyl ether at 20℃; for 72h; an autoclave;
  • 9
  • [ 13269-52-8 ]
  • [ 4984-85-4 ]
  • [ 922-17-8 ]
YieldReaction ConditionsOperation in experiment
78% With tert.-butylhydroperoxide; tetraethylammonium acetate In water; toluene; acetonitrile at 0℃; for 18h; Yields of byproduct given;
1: 40% 2: 50% With tert.-butylhydroperoxide In water; toluene; acetonitrile at 0℃;
  • 10
  • [ 4984-85-4 ]
  • [ 100-39-0 ]
  • [ 73172-48-2 ]
YieldReaction ConditionsOperation in experiment
64% With sodium hydroxide In water; dimethyl sulfoxide
  • 11
  • [ 4984-85-4 ]
  • [ 124-63-0 ]
  • [ 102096-18-4 ]
YieldReaction ConditionsOperation in experiment
57% With triethylamine In diethyl ether for 0.5h;
With triethylamine In diethyl ether at 0℃; for 5.5h;
  • 12
  • [ 4984-85-4 ]
  • [ 106-95-6 ]
  • [ 73172-49-3 ]
YieldReaction ConditionsOperation in experiment
62% With sodium hydroxide In water; dimethyl sulfoxide
  • 13
  • [ 4984-85-4 ]
  • [ 62-56-6 ]
  • [ 70253-96-2 ]
YieldReaction ConditionsOperation in experiment
25% With hydrogenchloride In various solvent(s) for 2h; Heating;
25% In various solvent(s) for 5h; Heating;
 

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• Appel Reaction • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Heat of Combustion • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Lawesson's Reagent • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Specialized Acylation Reagents-Ketenes • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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