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Sodium borohydride → 2-(((4-Methoxyphenyl)methyl)amino)propan-1-ol

HRID 716978
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 716978
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6](/[CH:7]=[N:8]/[CH:9]([CH3:12])[CH2:10][OH:11])=[CH:5][CH:4]=1.[BH4-].[Na+]>CO>[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]([CH2:7][NH:8][CH:9]([CH3:12])[CH2:10][OH:11])=[CH:5][CH:4]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 4311764Sodium borohydrideHCID 178491096HCID 178491096, Verbindung

Produkt 1

HCID 222898522-(((4-Methoxyphenyl)methyl)amino)propan-1-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
-5 °C

Versuchsvorschrift

Into a 250-mL 3-necked round-bottom flask, was placed a solution of (E)-2-(4-methoxybenzylideneamino)propan-1-ol (15 g, 77.72 mmol, 1.00 equiv) in methanol (150 mL). This was followed by the addition of NaBH4 (5.88 g, 155.56 mmol, 2.00 equiv) in several batches at −10-0° C. The resulting solution was stirred for 2 hs at −10-0° C. in an ice/salt bath. The resulting mixture was concentrated under vacuum and diluted with 200 mL of water. The resulting aqueous solution was extracted with 3×100 mL of ethyl acetate and the organic layers was combined and dried over anhydrous magnesium sulfate, concentrated under vacuum. This resulted in 11.1 g (73%) of 2-(4-methoxybenzylamino)propan-1-ol as a white solid.

Aufarbeitung

  1. customInto a 250-mL 3-necked round-bottom flask, was placed
  2. concentrationThe resulting mixture was concentrated under vacuum
  3. additiondiluted with 200 mL of water
  4. extractionThe resulting aqueous solution was extracted with 3×100 mL of ethyl acetate
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated under vacuum
  7. customThis resulted in 11.1 g (73%) of 2-(4-methoxybenzylamino)propan-1-ol as a white solid

Quellen und Nachweise

ORD-Eintrag
ord-05375b7d48654272b367aa1deadb39fc
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09193693B2

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