Hydrochloric Acid → Ethyl-4-(3-isopropyl-2-methoxyphenyl)-4-methyl-2-oxo-pentanoate

HRID 1443235Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1443235
[Sn](Cl)(Cl)(Cl)Cl.[CH:6]([C:9]1[C:10]([O:19][CH3:20])=[C:11]([C:15](O)([CH3:17])[CH3:16])[CH:12]=[CH:13][CH:14]=1)([CH3:8])[CH3:7].[CH2:21]([O:23][C:24](=[O:32])[C:25]([O:27][Si](C)(C)C)=[CH2:26])[CH3:22].C(=O)([O-])[O-].[Na+].[Na+].Cl>ClCCl.O>[CH2:21]([O:23][C:24](=[O:32])[C:25](=[O:26])[CH2:27][C:15]([C:11]1[CH:12]=[CH:13][CH:14]=[C:9]([CH:6]([CH3:8])[CH3:7])[C:10]=1[O:19][CH3:20])([CH3:17])[CH3:16])[CH3:22]

Komponenten

8

Edukt 5

HCID 313Hydrochloric AcidHCID 10340Sodium Carbonate2×HCID 24287Tin tetrachlorideHCID 111168062-Trimethylsilanyloxy-acrylic acid ethyl esterHCID 179891992-(3-Isopropyl-2-methoxyphenyl)propan-2-ol

Produkt 1

HCID 17989132Ethyl-4-(3-isopropyl-2-methoxyphenyl)-4-methyl-2-oxo-pentanoateAusbeute 49,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel2×HCID 6344DichloromethaneLösungsmittel3×

Reaktionsbedingungen

Temperatur
-72 °C

Versuchsvorschrift

15.3 ml (129.71 mmol) of tin tetrachloride is added in drops to a mixture, cooled to −72° C., that consists of 28.16 g (135.19 mmol) of 2-(3-isopropyl-2-methoxyphenyl)-propan-2-ol and 50.9 g (270.38 mmol) of 2-trimethylsilanyloxy-acrylic acid ethyl ester in 420 ml of dichloromethane. In this case, the temperature increased to −65° C. After 30 minutes of stirring in this temperature interval, the reaction mixture is poured onto a mixture that consists of saturated sodium carbonate solution and dichloromethane (in each case 250 ml). After 30 minutes of stirring at room temperature, the batch is transferred into a spherical separating funnel, and a 1:1 mixture that consists of water and dichloromethane is added until a phase separation takes place. After the organic phase is shaken with sodium carbonate, 1N HCl and water, it is dried with sodium sulfate. After the usual procedure, the residue is chromatographed on silica gel (mobile solvent: ethyl acetate/hexane). 20.44 g (48.35%) of the desired compound is obtained.

Aufarbeitung

  1. temperatureIn this case, the temperature increased to −65° C
  2. additionthe reaction mixture is poured onto a mixture that
  3. stirringAfter 30 minutes of stirring at room temperature
  4. customthe batch is transferred into a spherical separating funnel
  5. additionis added until a phase separation
  6. dry with materialis dried with sodium sulfate
  7. customAfter the usual procedure, the residue is chromatographed on silica gel (mobile solvent: ethyl acetate/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-ef13a7846ab1487e8c46e74cbb13d7ca
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07659297B2

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