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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27151Erstellt: 24. Oktober 2026

1-Butanol → 1-(N-benzyloxycarbonyl-m-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

https://huagongshe.com/de/reaction/27151

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-ButanolHCID 263—
EduktDopamine HydrochlorideHCID 65340—
EduktN-benzyloxycarbonyl-m-fluoroanilinoacetaldehyde diethyl acetalHCID 20460585—
LösungsmittelWaterHCID 962—
Produkt1-(N-benzyloxycarbonyl-m-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 2046054981%

Reaktionsschritte

N-benzyloxycarbonyl-m-fluoroanilinoacetaldehyde diethyl acetal (15 g) and 3,4-dihydroxyphenethylamine hydrochloride (5.75 g) were added to a mixture of n-butyl alcohol (150 ml) and water (20 ml) and then the mixture was refluxed for 11 hours in a stream of nitrogen. The reaction mixture was concentrated to dryness and the residue was in turn washed with ether and with a mixture of ether: ethyl acetate (2:1) and then crystallized with acetone. The crystals were collected by filtration to give 1-(N-benzyloxycarbonyl-m-fluoroanilinomethyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride (11.27 g), mp 184° to 186° C. (dec).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04220647
Quelldatensatzuspto-grants-1980_09
ORD IDord-3721dd1e793345b5afbf9545d29a7c99
Quellennotizuspto-grants-1980_09