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
6
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
- customThe resulting reaction mixture
- filtrationwas filtered
- customto remove the catalyst
- customThe filtrate was evaporated under vacuum
- customto remove ammonia
- dissolutionThe residue was dissolved in a 1:1 mixture of 2-butanol and tetrahydrofuran
- additiontreated with activated carbon
- 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
- 特許番号
- US08653306B1
関連ノート
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