Sodium borohydride → 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ol

HRID 274080Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 274080
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]2[CH2:7][CH2:8][CH2:9][C:10](=[O:12])[CH2:11][C:5]=2[CH:4]=1.[BH4-].[Na+]>CO>[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]2[CH2:7][CH2:8][CH2:9][CH:10]([OH:12])[CH2:11][C:5]=2[CH:4]=1

Komponenten

4

Edukt 2

HCID 4311764Sodium borohydrideHCID 105595743-Methoxy-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-one

Produkt 1

HCID 200947203-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-one (220 g) in methanol (1300 ml) was added portionwise sodium borohydride (22.0 g) at 6° C.-30° C., and then the reaction mixture was stirred for 40 minutes and evaporated in vacuo. The residue was partitioned between ethyl acetate (1 l) and water (1 l). The organic layer was washed with 1N hydrochloric acid (500 ml), aqueous sodium hydrogen carbonate (500 ml), and brine (200 ml), and dried over magnesium sulfate. The solvent was evaporated in vacuo to give 3-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ol as a white powder.

Aufarbeitung

  1. customevaporated in vacuo
  2. customThe residue was partitioned between ethyl acetate (1 l) and water (1 l)
  3. washThe organic layer was washed with 1N hydrochloric acid (500 ml), aqueous sodium hydrogen carbonate (500 ml), and brine (200 ml)
  4. dry with materialdried over magnesium sulfate
  5. customThe solvent was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-0361da08f81c4e1da779d4da0c028911
Quelldatensatz
uspto-grants-1995_02
Patentnummer
US05387710

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