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Dichloromethane → HCID 136341362, Verbindung

HRID 627728
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 627728
[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][C:8]([O:12]C)=[CH:7]2.B(Br)(Br)Br.ClCCl>ClCCCl>[Cl:1][C:2]1[N:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[CH:9][C:8]([OH:12])=[CH:7]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6344DichloromethaneHCID 25134Boron tribromideHCID 867157508-Chloro-3-methoxy-1,7-naphthyridine

Produkt 1

HCID 136341362HCID 136341362, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 111,2-DichloroethaneLösungsmittel

Versuchsvorschrift

To a 75 mL pressure vessel were charged with 8-chloro-3-methoxy-1,7-naphthyridine (0.8 g, 4.11 mmol) and DCE (10 ml). To this was added boron tribromide, 1.0M in dichloromethane (20.55 ml, 20.55 mmol) slowly. The brown heterogeneous mixture was stirred at RT and then was heated to 60° C. in oil bath and stirred for 3 h. It was cooled to 0° C. by ice bath and quenched with sat. Na2CO3 very slowly. Organic solvents were reduced, and 100 ml EtOH was added to the resulting residue. The white precipitate was filtered out. The filtrate was concentrated to yield 8-chloro-1,7-naphthyridin-3-ol as crude product which was used for next step directly. MS m/z: 181.2 [M+H].

Aufarbeitung

  1. temperaturewas heated to 60° C. in oil bath
  2. stirringstirred for 3 h
  3. temperatureIt was cooled to 0° C. by ice bath
  4. customquenched with sat. Na2CO3 very slowly
  5. addition100 ml EtOH was added to the resulting residue
  6. filtrationThe white precipitate was filtered out
  7. concentrationThe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-c4698a01461946cfadd9240109f6a457
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09309263B2

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