Thionyl Chloride → 4-Chloro-6-(chloromethyl)-1,3-dioxaindane

HRID 468276Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 468276
[Cl:1][C:2]1[C:7]2[O:8][CH2:9][O:10][C:6]=2[CH:5]=[C:4]([CH2:11]O)[CH:3]=1.O=S(Cl)[Cl:15]>ClCCl>[Cl:1][C:2]1[C:7]2[O:8][CH2:9][O:10][C:6]=2[CH:5]=[C:4]([CH2:11][Cl:15])[CH:3]=1

Komponenten

4

Edukt 2

HCID 24386Thionyl ChlorideHCID 4962440(7-Chloro-1,3-dioxaindan-5-yl)methanol

Produkt 1

HCID 162270934-Chloro-6-(chloromethyl)-1,3-dioxaindane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A mixture of (7-chlorobenzo[d][1,3]-dioxol-5-yl)methanol (5.5 g, 30 mmol) and SOCl2 (5.0 mL, 67 mmol) in dichloromethane (20 mL) was stirred at room temperature for 1 h and was then poured into ice water. The organic layer was separated and the aqueous phase was extracted with dichloromethane (50 mL×3). The combined extracts were washed with water and aqueous NaHCO3 solution, dried over Na2SO4 and evaporated under reduced pressure to afford 4-chloro-6-(chloromethyl)benzo[d][1,3]dioxole, which was directly used in the next step.

Aufarbeitung

  1. customThe organic layer was separated
  2. extractionthe aqueous phase was extracted with dichloromethane (50 mL×3)
  3. washThe combined extracts were washed with water and aqueous NaHCO3 solution
  4. dry with materialdried over Na2SO4
  5. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-78d6089cccf74786b39b558a8104067a
Quelldatensatz
uspto-grants-2014_01
Patentnummer
US08623905B2

Notizen zur Reaktion

Wird geladen…