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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1417803Erstellt: 27. Oktober 2026

m-Chlorophenethylic alcohol → 6-Chloro-1-(2-chloroethyl)isochroman

https://huagongshe.com/reaction/1417803

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Chlorophenethylic alcoholHCID 78856—
Edukt3-Chloro-1,1-diethoxypropaneHCID 96217—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelNitromethaneHCID 6375—
Produkt6-Chloro-1-(2-chloroethyl)isochromanHCID 23288787—

Reaktionsschritte

A mixture of 3-chlorophenethyl alcohol (XLV, 5.9055 g, 0.0398 mol), 3-chloropropionaldehyde diethyl acetal (LXII, 7.2 ml, 0.0430 mol) and nitromethane (3 ml) is cooled in an ice/water bath. Titanium tetrachloride (1M in dichloromethane, 88 ml, 0.088 mol) is added dropwise and the mixture is heated at 45° for 3 hr. After cooling, the mixture is poured onto ice/aqueous hydrochloric acid (1N) and extracted with dichloromethane. The combined organic layers are backwashed with hydrochloric acid (1N) and filtered through a pad of Celite topped with sodium sulfate. The filtrate is concentrated and chromatographed twice on silica gel eluting with ethyl acetate/hexane (5/95). The appropriate fractions are pooled and concentrated to give 6-chloro-1-(2-chloroethyl)isochroman (LXIV), NMR (CDCl3) 2.23, 2.70, 2.93, 3.75, 4.09, 4.89, 7.01 and 7.16 δ.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05877317
Quelldatensatzuspto-grants-1999_03
ORD IDord-cce3a20a57c24e909d4c8860f4672f44
Quellennotizuspto-grants-1999_03