Benzyl Alcohol → HCID 18370146, Verbindung

HRID 484752Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 484752
[CH3:1][CH:2]([CH3:10])[CH2:3][CH2:4][C:5](=[O:9])[C:6]([OH:8])=[O:7].C1(N=C=NC2CCCCC2)CCCCC1.[CH2:26](O)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>C(Cl)Cl>[CH3:1][CH:2]([CH3:10])[CH2:3][CH2:4][C:5](=[O:9])[C:6]([O:8][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)=[O:7]

Komponenten

5

Reaktionsbedingungen

Temperatur
-15 °C

Versuchsvorschrift

A solution of 5-methyl-2-oxohexanoic acid (0.288 g.) in methylene chloride (1 ml.) was added during 15 minutes to a stirred solution of dicyclohexylcarbodiimide (0.412 g.) and benzyl alcohol (0.432 g.) in methylene chloride (10 ml.) which was cooled to -15° C., and the mixture was stirred at that temperature for 1 hour, then at laboratory temperature for 30 minutes, and was then evaporated to dryness. Water (1 ml.), diethyl ether (2 ml.) and acetic acid (0.01 ml.) were added and the mixture was kept at laboratory temperature for 12 hours and then evaporated to dryness. The residue was purified by chromatography on a silica gel column using toluene as eluant and there was thus obtained benzyl 5-methyl-2-oxohexanoate as an oil.

Aufarbeitung

  1. waitat laboratory temperature for 30 minutes
  2. customwas then evaporated to dryness
  3. additionWater (1 ml.), diethyl ether (2 ml.) and acetic acid (0.01 ml.) were added
  4. waitthe mixture was kept at laboratory temperature for 12 hours
  5. customevaporated to dryness
  6. customThe residue was purified by chromatography on a silica gel column

Quellen und Nachweise

ORD-Eintrag
ord-80e098dd023b4de6a0e2fa2858024579
Quelldatensatz
uspto-grants-1985_08
Patentnummer
US04533656

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