Vinyl Acetate → (R)-1-acetoxyindene

HRID 3010

Reaktionsgleichung

Reaktionsgleichung von HRID 3010
[CH:1]1([OH:10])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[C:11](OC=C)(=[O:13])[CH3:12]>C(OC)(C)(C)C>[C:11]([O:10][C@H:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1)(=[O:13])[CH3:12].[C@@H:1]1([OH:10])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1

Komponenten

5

Edukt 2

HCID 7904Vinyl AcetateHCID 316919Indenol

Produkt 2

HCID 12414573(1s)-IndenolAusbeute 10 %HCID 12414574(R)-1-acetoxyindeneAusbeute 38 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 15413tert-Butyl methyl etherLösungsmittel

Reaktionsbedingungen

Temperatur
37 °C

Versuchsvorschrift

100 mg (0.76 mmol) of racemic inden-1-ol, 0.13 mg (1.15 mmol) of vinyl acetate and 75.6 mg (100 mg of racemate/mmol) of lipase PS were suspended in 10 ml of t-butylmethyl ether and stirred at 37° C. for 7 days. After the end of the reaction, the suspension was filtered off to remove lipase. The filtrate was concentrated and the residue was subjected to silica gel column chromatography (eluate: ethyl acetate-hexane, 1:10 V/V), to separate into 50 mg (yield 38.0%, optical purity 22% ee) of (R)-1-acetoxyindene and 10 mg (yield 10.0%, optical yield 22% ee) of (S)-inden-1-ol respectively. The optical purities were determined by an analysis according to high speed liquid chromatography (column: chiral cell OD, eluate: isopropanol-hexane, 1% V/V).

Aufarbeitung

  1. customAfter the end of the reaction
  2. filtrationthe suspension was filtered off
  3. customto remove lipase
  4. concentrationThe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-a52c34c433e043df8e5ada85e1f85e19
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05731464

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