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Dihydroxyacetone → 2-((1,3-Dihydroxypropan-2-yl)amino)propane-1,3-diol

HRID 243756
ノート
印刷プレビュー

反応式

HRID 243756 の反応式
[NH2:1][CH:2]([CH2:5][OH:6])[CH2:3][OH:4].[OH:7][CH2:8][C:9]([CH2:11][OH:12])=O.[H][H]>[Ni].CO>[NH:1]([CH:9]([CH2:11][OH:12])[CH2:8][OH:7])[CH:2]([CH2:5][OH:6])[CH2:3][OH:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 670DihydroxyacetoneHCID 68294SerinolHCID 178418361HCID 178418361、化合物

生成物 1

HCID 107021932-((1,3-Dihydroxypropan-2-yl)amino)propane-1,3-diol収率 79%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 887Methanol溶媒

実験手順

In an autoclave, a mixture of serinol (10.6 g, 0.12 mol), 1,3-dihydroxyacetone (10.4 g, 0.12 mol), and Raney nickel (1 g, wet) in methanol (100 ml) was heated to 65° C. under 250 psi hydrogen pressure for 3 h. The autoclave was cooled to ambient temperature and depressurized. The resulting reaction mixture was filtered to remove the catalyst. The filtrate was evaporated under vacuum to remove ammonia and most of the water. The residue was dissolved in a 1:1 mixture of 2-butanol and tetrahydrofuran, treated with activated carbon, and evaporated to give the bis-adduct 2,2′-iminobis-1,3-propanediol as a viscous oil (15 g, 79%). Assay by GC: 99%.

後処理

  1. customThe resulting reaction mixture
  2. filtrationwas filtered
  3. customto remove the catalyst
  4. customThe filtrate was evaporated under vacuum
  5. customto remove ammonia
  6. dissolutionThe residue was dissolved in a 1:1 mixture of 2-butanol and tetrahydrofuran
  7. additiontreated with activated carbon
  8. customevaporated

出典と根拠

ORDレコード
ord-f1810db1922e409eb2041b56b26a981f
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08653306B1

反応ノート

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