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

HRID 1165673
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HRID 1165673 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

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

생성물 1

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

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-672692f460ef4cdaacd08a5d79c75c01
출처 데이터셋
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04910218

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