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

HRID 1964796
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1964796
[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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

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

Produkt 1

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

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 11
1,2-Dichloroethane
Lösungsmittel

Versuchsvorschrift

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%).

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-9be17ea6be714fdbbf3333201b4abd9a
Quelldatensatz
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08415480B2

Notizen zur Reaktion

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