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(Phenylmethoxy)acetaldehyde → HCID 19922573, Verbindung

HRID 1647933
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1647933
[CH2:1]([S:3][C:4]([O:6][Si](C)(C)C)=[CH2:5])[CH3:2].[CH2:11]([O:18][CH2:19][CH:20]=[O:21])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.Cl.CO>C1(C)C=CC=CC=1>[CH2:11]([O:18][CH2:19][CH:20]([OH:21])[CH2:6][C:4](=[O:5])[S:3][CH2:1][CH3:2])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 108989(Phenylmethoxy)acetaldehydeHCID 11008467Silane, [[1-(ethylthio)ethenyl]oxy]trimethyl-HCID 21893726Hydrochloride methanol

Produkt 1

HCID 19922573HCID 19922573, VerbindungAusbeute 84 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

To a solution of 21.5 mg (0.05 mmol) of (R)-1 in 3 ml of toluene were added 176 mg (1 mmol) of 1-ethylthio-1-(trimethylsilyl)oxyethene and 150 mg (1 mmol) of α-benzyloxyacetaldehyde at 0° C. After stirring for 2 hours at that temperature, the resultant mixture was poured into 10 ml of a buffer (pH 7) at 0° C. The solution was filtered through a pad of Celite, and the filtrate was extracted three times with a 5 ml portion of diethyl ether. The combined organic layer was washed with brine, dried over magnesium sulfate, and evaporated under reduced pressure to give a crude product in a silylated form. The crude product was poured into 10% hydrochloric acid-methanol, and the mixture was purified by silica gel chromatography (eluent: hexane/ethyl acetate=20/1 by volume) to obtain S-ethyl 4-benzyloxy-3-hydroxybutanethioate in a yield of 84%.

Aufarbeitung

  1. filtrationThe solution was filtered through a pad of Celite
  2. extractionthe filtrate was extracted three times with a 5 ml portion of diethyl ether
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated under reduced pressure
  6. customto give a crude product in a silylated form
  7. customthe mixture was purified by silica gel chromatography (eluent: hexane/ethyl acetate=20/1 by volume)

Quellen und Nachweise

ORD-Eintrag
ord-e81ec7534ad64f2ebc1bd3092117ca4a
Quelldatensatz
uspto-grants-1995_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05434289

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