Methanol → 3-(3-Chloro-benzo[b]thiophen-2-yl)-propan-1-ol

HRID 2264637Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2264637
C[O:2][C:3](=O)[CH2:4][CH2:5][C:6]1[S:10][C:9]2[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=2[C:7]=1[Cl:15].[Li+].[BH4-].CO.[OH-].[Na+]>CCOCC>[Cl:15][C:7]1[C:8]2[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=2[S:10][C:6]=1[CH2:5][CH2:4][CH2:3][OH:2]

Komponenten

6

Edukt 4

HCID 887MethanolHCID 14798Sodium HydroxideHCID 4148881Lithium borohydrideHCID 667607513-(3-Chloro-benzo[b]thiophen-2-yl)-propionic acid methyl ester

Produkt 1

HCID 219644313-(3-Chloro-benzo[b]thiophen-2-yl)-propan-1-olAusbeute 79 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

An ice cold solution of 3.63 g (14.3 mmol) of 15 in 60 mL of ether was treated with LiBH4 (621 mg, 28.5 mmol) and methanol (2 mL). After 30 min., 30 mL of 0.5 M NaOH solution was added. The mixture was extracted with ethyl acetate (2×25 mL) and the combined ethyl acetate solution washed with brine (50 mL), dried (MgSO4), filtered and evaporated. The residue was purified by flash chromatography on silica gel (5-20% ethyl acetate/hexane) to give 2.57 g (11.3 mmol, 79%) of the alcohol (16).

Aufarbeitung

  1. extractionThe mixture was extracted with ethyl acetate (2×25 mL)
  2. washthe combined ethyl acetate solution washed with brine (50 mL)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customevaporated
  6. customThe residue was purified by flash chromatography on silica gel (5-20% ethyl acetate/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-ce80c7a4c9fc4967b9088b40be903387
Quelldatensatz
uspto-grants-2010_12
Patentnummer
US07855226B2

Notizen zur Reaktion

Wird geladen…