Thionyl Chloride → 2,4-Dibenzyloxyphenylacetyl chloride

HRID 2073567Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2073567
[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:12]=[CH:11][C:10]=1[CH2:23][C:24]([OH:26])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:29])=O>C1C=CC=CC=1>[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:12]=[CH:11][C:10]=1[CH2:23][C:24]([Cl:29])=[O:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

4

Edukt 2

HCID 24386Thionyl ChlorideHCID 50283782-[2,4-Bis(benzyloxy)phenyl]acetic Acid

Produkt 1

HCID 138730072,4-Dibenzyloxyphenylacetyl chloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

2,4-Dibenzyloxyphenylacetic acid [IX] (1.4 g) was dissolved in anhydrous benzene (30 ml) and then thereto was added thionyl chloride (5 g) and the mixture was left to stand at room temperature (20° C.) for 20 minutes. The reaction mixture was concentrated to dryness under reduced pressure to obtain crude 2,4-dibenzyloxyphenylacetyl chloride [X]. This was used for the subsequent reaction without purification.

Aufarbeitung

  1. waitthe mixture was left
  2. customto stand at room temperature
  3. custom(20° C.)
  4. customfor 20 minutes
  5. concentrationThe reaction mixture was concentrated to dryness under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-6a910550abf546b2aa0050721bd44d49
Quelldatensatz
uspto-grants-1990_04
Patentnummer
US04918107

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