1,3-Dibromobenzene → 1-(3-Bromophenyl)-cyclobutanol

HRID 1276525Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1276525
Br[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Br:8])[CH:3]=1.C([Li])CCC.[C:14]1(=[O:18])[CH2:17][CH2:16][CH2:15]1>O1CCCC1.CCCCCC>[Br:8][C:4]1[CH:3]=[C:2]([C:14]2([OH:18])[CH2:17][CH2:16][CH2:15]2)[CH:7]=[CH:6][CH:5]=1

Komponenten

6

Edukt 3

HCID 79271,3-DibromobenzeneHCID 14496CyclobutanoneHCID 178418339Butyllithium

Produkt 1

HCID 184615711-(3-Bromophenyl)-cyclobutanolAusbeute 66,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittelHCID 8058HexaneLösungsmittel

Versuchsvorschrift

To a solution of 1,3-dibromo-benzene (2.36 grams, 10 mmol) in tetrahydrofuran at -78° C. was added a 1.6M solution of n-butyllithium (6.3 ml, 10 mmol) in hexane and stirred for 4 hours. Cyclobutanone (700 mg, 10 mmol) was then added in one portion. After stirring for 2 hours at -78° C., the reaction was quenched with 2N hydrochloric acid. The reaction was warmed to room temperature, diluted with water and extracted with ethyl acetate. The ethyl acetate layer was dried and evaporated to give 2.5 grams of crude product which was purified on silica gel eluting with 50% methylene chloride in hexane to give 1.5 grams of the titled compound.

Aufarbeitung

  1. stirringAfter stirring for 2 hours at -78° C.
  2. customthe reaction was quenched with 2N hydrochloric acid
  3. additiondiluted with water
  4. extractionextracted with ethyl acetate
  5. dry with materialThe ethyl acetate layer was dried
  6. customevaporated
  7. customto give 2.5 grams of crude product which
  8. customwas purified on silica gel eluting with 50% methylene chloride in hexane

Quellen und Nachweise

ORD-Eintrag
ord-b433bcd288e5428f95e3795ff0d70b0f
Quelldatensatz
uspto-grants-2000_12
Patentnummer
US06166064

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