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HRID 1414Erstellt: 23. Oktober 2026

Hydrochloric Acid → 6-Benzyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid

https://huagongshe.com/de/reaction/1414

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBenzyl BromideHCID 7498—
EduktPotassium HydroxideHCID 14797—
Edukt6-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 19070001—
KatalysatorSodium IodideHCID 5238—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt6-Benzyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic AcidHCID 1906997392,8%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 10.60 g (50 mmol) of 1,2,3,4-tetrahydro-6-hydroxynaphthalene-2-carboxylic acid, 12.85 g (75 mmol) of benzyl bromide, 6.6 g (100 mmol) of 85% potassium hydroxide, 0.525 g (3.5 mmol) of sodium iodide, 200 ml of ethanol and 25 ml of distilled water was heated under reflux at 100° C. for 12 hours. To this reaction mixture was added 50 ml of 10% potassium hydroxide, followed by heating under reflux at that temperature for 2 hours. After allowing the reaction system to cool up to room temperature, the reaction mixture in cold water was acidified with 36% hydrochloric acid. The resulting deposited product was filtered, and recrystallized from toluene to obtain 13.08 g (46.4 mmol) of 1,2,3,4-tetrahydro-6-benzyloxynaphthalene-2-carboxylic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05725798
Quelldatensatzuspto-grants-1998_03
ORD IDord-7d2c74c555f047899e0fbc54d1163d31
Quellennotizuspto-grants-1998_03