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Ethanolamine → 2-[(2-Furylmethyl)amino]ethanol

HRID 1964796
ノート
印刷プレビュー

反応式

HRID 1964796 の反応式
[CH:1]1[CH:5]=[C:4]([CH:6]=O)[O:3][CH:2]=1.[NH2:8][CH2:9][CH2:10][OH:11].C[C@H](NC([C@H]1N(C([C@@H](NC([C@@H](N)CC2C=CC(O)=CC=2)=O)CC(O)=O)=O)CCC1)=O)C(N1[C@H](C(N2[C@H](C(N3[C@H](C(N4[C@H](C(N5[C@H](C(N6[C@H](C(O)=O)CCC6)=O)CCC5)=O)CCC4)=O)CCC3)=O)CCC2)=O)CCC1)=O.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>ClCCCl>[O:3]1[CH:2]=[CH:1][CH:5]=[C:4]1[CH2:6][NH:8][CH2:9][CH2:10][OH:11]
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 4

HCID 700EthanolamineHCID 7362FurfuralHCID 5049666Sodium triacetoxyborohydrideHCID 5488810Peptide oostatic hormone

生成物 1

HCID 47226102-[(2-Furylmethyl)amino]ethanol

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

An aldehyde, e.g., 2-furfuraldehyde (2 g, 20.82 mmol), and an amine, e.g., 2-aminoethanol, (1.65 g, 27.06 mmol) were poured together in a mixture 1:1 TMOF:DCE (50 ml) and the reaction mixture was cooled down to zero degree. The reducing agent NaBH(OAc)3 (6.18 g, 29.14 mmol) was added in 4 subsequent portions over a 5 min period, the reaction mixture was allowed to gradually warm to room temperature and stirred for 16 hours. The solvents was removed from the reaction in vacuo and the residue was partitioned between dichloromethane (150 ml) and saturated bicarbonate solution (50 ml). After separation, the organic layer was washed with saturated bicarbonate solution (50 ml) and brine (50 ml). The combined organic layers were then dried over sodium sulphate, filtered and the solvent removed in vacuo. The desired secondary amines, e.g., 2-[(2-furylmethyl)amino]ethanol, were obtained as a yellowish oil (1.82 g, 62%).

後処理

  1. customThe solvents was removed from the reaction in vacuo
  2. customthe residue was partitioned between dichloromethane (150 ml) and saturated bicarbonate solution (50 ml)
  3. customAfter separation
  4. washthe organic layer was washed with saturated bicarbonate solution (50 ml) and brine (50 ml)
  5. dry with materialThe combined organic layers were then dried over sodium sulphate
  6. filtrationfiltered
  7. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-9be17ea6be714fdbbf3333201b4abd9a
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08415480B2

反応ノート

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