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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 28263Erstellt: 23. Oktober 2026

Hydrochloric Acid → (2-Chlorophenyl)(4-chlorophenyl)methanol

https://huagongshe.com/de/reaction/28263

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-ChlorobenzaldehydeHCID 6996—
Eduktp-BromochlorobenzeneHCID 7806—
EduktMagnesiumHCID 5462224—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(2-Chlorophenyl)(4-chlorophenyl)methanolHCID 247332—

Reaktionsschritte

To 12.7 g. (0.52 moles) of magnesium turnings in 200 ml. of anhydrous ether is added 10.0 g. (0.052 moles) of p-bromochlorobenzene, and the mixture is warmed to reflux. When the Grignard reaction begins, the heat is removed and 80.0 g. (0.47 moles) of additional p-bromochlorobenzene in 80 ml. of ether is added dropwise as the refluxing continues. When the addition is completed, the reaction is heated at reflux for 2 hours, cooled, and 73.4 g. (0.52 moles) of o-chlorobenzaldehyde are slowly added. The reaction is refluxed for 2 hours, cooled and poured into iced water. The resulting mixture is made acidic with hydrochloric acid, and the organic phase is separated. The aqueous layer is extracted with ether, and the extract is added to the organic phase. This solution is washed with water, dried over anhydrous magnesium sulfate and concentrated to give an oily solid. The material is crystallized from petroleum ether to give 109.4 g. (83%) of the product, mp 68°-70°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04225723
Quelldatensatzuspto-grants-1980_09
ORD IDord-d1fb74da1fe1496a9557c93116c7aab5
Quellennotizuspto-grants-1980_09