Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1288461Erstellt: 25. Oktober 2026

Sulfur Dioxide → 2-Acetyl-8-chlorosulfonyl-7-chloro-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1288461

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfur DioxideHCID 1119—
EduktNitrous AcidHCID 24529—
EduktMagnesium ChlorideHCID 5360315—
Edukt2-Acetyl-8-amino-7-chloro-1,2,3,4-tetrahydroisoquinolineHCID 20523214—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
Produkt2-Acetyl-8-chlorosulfonyl-7-chloro-1,2,3,4-tetrahydroisoquinolineHCID 12838041—

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

2-Acetyl-8-amino-7-chloro-1,2,3,4-tetrahydroisoquinoline (0.04 mole) in concentrated hydrochloric acid (8.4 ml.) is cooled to 3° C. and treated with sodium nitrite (0.044 mole) dissolved in water (6 ml.). After stirring for 30 minutes, the reaction is tested for nitrous acid with starch/iodide paper. If the test for nitrous acid is negative, more sodium nitrite is added in small portions with stirring over a period of time until the test is positive. When a positive reaction is obtained, magnesium chloride (0.032 mole) is added and the resulting mixture is added to a mixture of acetic acid (40 ml.) saturated with sulfur dioxide and cuprous chloride dihydrate (0.0129 mole) maintained at 30° C. and stirred. After about 30 minutes, the mixture is diluted with water (60 ml.) and extracted with ether. The extract is then washed with dilute aqueous sodium bicarbonate/sodium carbonate solution at pH 8-9, then with water, and dried over sodium sulfate. The ether is evaporated to yield 2-acetyl-8-chlorosulfonyl-7-chloro-1,2,3,4-tetrahydroisoquinoline.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03988339
Quelldatensatzuspto-grants-1976_10
ORD IDord-0cf1bb2f5c0b42889e527665e590cf69
Quellennotizuspto-grants-1976_10