Hydrochloric Acid → 2,4,6-trimethyl-1H-indene

HRID 1728786Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1728786
[CH3:1][CH:2]1[CH2:10][C:9]2[C:4](=[C:5]([CH3:12])[CH:6]=[C:7]([CH3:11])[CH:8]=2)[C:3]1=O.[BH4-].[Na+].Cl>O1CCCC1>[CH3:1][C:2]1[CH2:10][C:9]2[C:4]([CH:3]=1)=[C:5]([CH3:12])[CH:6]=[C:7]([CH3:11])[CH:8]=2

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 4311764Sodium borohydrideHCID 117690492,5,7-Trimethyl-1-indanone

Produkt 1

HCID 109207862,4,6-trimethyl-1H-indeneAusbeute 96 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

20.4 g (117 mmol) of 2,5,7-trimethyl-1-indanone (1) were dissolved in 300 ml of a mixture of tetrahydrofuran/-methanol (2:1), and 6.6 g (175 mmol) of NaBH4 were added at room temperature. The mixture was stirred for a further hour, 50 ml of half-concentrated HCl were added and the mixture was extracted with ether. The combined organic phases were dried over sodium sulfate and freed from the solvent. The residue was transferred to a distillation apparatus, and 13 g of magnesium sulfate were added. A vacuum of about 10 mbar was applied and the mixture was heated up until the product distilled over (130°-150° C.). The distillation gave 17.7 g of the indene 2 as a colorless oil. The yield was 96%.

Aufarbeitung

  1. additionwere added at room temperature
  2. extractionthe mixture was extracted with ether
  3. dry with materialThe combined organic phases were dried over sodium sulfate
  4. additionwere added
  5. temperaturethe mixture was heated up until the product
  6. distillationdistilled over (130°-150° C.)
  7. distillationThe distillation

Quellen und Nachweise

ORD-Eintrag
ord-21682be6e726452ebd2569592ee916fe
Quelldatensatz
uspto-grants-1994_07
Patentnummer
US05328969

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