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

HRID 620527
ノート
印刷プレビュー

反応式

HRID 620527 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

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

生成物 1

HCID 1438812-Nitro-2-isopropyl-1,3-propanediol収率 87%

実験手順

A solution of 2-methyl-1-nitropropane (38.7 g, 0.375 mol prepared by the procedure of N. Kornblum, B. Taube, and H. Ungnade, J. Am. 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 a waxy, white solid mp 67°-72° (lit. mp 87°-88°, B. M. Vanderbilt and H. B. Hass, Ind. Eng. Chem. 32, 34 (1940). In our hands this procedure failed to give the desired compound).

後処理

  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

出典と根拠

ORDレコード
ord-9381758d3c8d4d1e805f7cd2ada79ffb
出典データセット
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04820873

反応ノート

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