StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Methyl 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylate → 7-Chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylic acid

HRID 1868356
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1868356
[Cl:1][C:2]1[CH:3]=[C:4]([C:14]([O:16]C)=[O:15])[C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[C:11]=1[O:12][CH3:13]>[OH-].[Na+]>[Cl:1][C:2]1[CH:3]=[C:4]([C:14]([OH:16])=[O:15])[C:5]2[O:10][CH2:9][CH2:8][O:7][C:6]=2[C:11]=1[O:12][CH3:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 11565132Methyl 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylate

Produkt 1

HCID 115939517-Chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylic acidAusbeute 2,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 14798Sodium HydroxideLösungsmittel

Versuchsvorschrift

A mixture of intermediate (2) (0.138 mol) in a 2N NaOH solution (500 ml) was stirred and refluxed for 1 hour, then cooled and washed with DCM. The mixture was separated into its layers. The aqueous layer was acidified with a concentrated HCl solution until pH=2. The solid was filtered off, washed with water and dried in vacuo. A part (2.5 g) of this fraction was crystallized from methanol. The precipitate was filtered off and dried, yielding 0.88 g of 7-chloro-2,3-dihydro-8-methoxy-1,4-benzodioxin-5-carboxylic acid (intermediate 3, mp. 172° C.).

Aufarbeitung

  1. temperaturerefluxed for 1 hour
  2. temperaturecooled
  3. washwashed with DCM
  4. customThe mixture was separated into its layers
  5. filtrationThe solid was filtered off
  6. washwashed with water
  7. customdried in vacuo
  8. customA part (2.5 g) of this fraction was crystallized from methanol
  9. filtrationThe precipitate was filtered off
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-331ee86488bb45b8aa2398f3db7e4946
Quelldatensatz
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07635706B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion