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Formaldehyde → 2-Nitro-2-isopropyl-1,3-propanediol

HRID 1165673
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1165673
[CH3:1][CH:2]([CH3:7])[CH2:3][N+:4]([O-:6])=[O:5].CCN(CC)CC.[CH2:15]=[O:16].[CH3:17][OH:18]>>[CH:2]([C:3]([N+:4]([O-:6])=[O:5])([CH2:17][OH:18])[CH2:15][OH:16])([CH3:7])[CH3:1]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 712FormaldehydeHCID 887MethanolHCID 8471TriethylamineHCID 693672-Methyl-1-nitropropane

Produkt 1

HCID 1438812-Nitro-2-isopropyl-1,3-propanediolAusbeute 87 %

Versuchsvorschrift

To a solution of 2-methyl-1-nitropropane (38.7 g, 0.375 mol, prepared by the procedure of N. Kornblum, B. Tunbe, and H. Ungnade, J. Amer. Chem. Soc., 76, 3209 (1954)) and NEt3 (Eastman, 3.79 g, 0.0375 mol) in CH3OH (50 mL) was added dropwise 37% aqueous formaldehyde solution (Mallinckrodt, 76.2 g, 0.938 mol) at a rate such that the reaction mixture temperature did not exceed 30°. After 72 h, the solution was concentrated under vacuum and the residue was dissolved in H2O (250 mL). The solution was continuously extracted for 1 h with CH2Cl2 (1 L). The CH2Cl2 solution was dried (MgSO4), filtered, and concentrated to give 53.3 g (87%) of 2-isopropyl-2-nitro-1,3-propanediol, as a waxy, white solid, mp 67°-72° C. (lit. mp 87°-88°, B. M. Vanderbilt and H. B. Hass, Ind. Eng. Chem. 32, 34 (1940). In our hands this literature procedure failed to give the desired compound).

Aufarbeitung

  1. customdid not exceed 30°
  2. concentrationthe solution was concentrated under vacuum
  3. dissolutionthe residue was dissolved in H2O (250 mL)
  4. extractionThe solution was continuously extracted for 1 h with CH2Cl2 (1 L)
  5. dry with materialThe CH2Cl2 solution was dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-672692f460ef4cdaacd08a5d79c75c01
Quelldatensatz
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04910218

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