HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1414Erstellt: 23. Oktober 2026
Hydrochloric Acid → 6-Benzyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid
https://huagongshe.com/de/reaction/1414
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 6-Hydroxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid | HCID 19070001 | — |
| Katalysator | Sodium Iodide | HCID 5238 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 6-Benzyloxy-1,2,3,4-tetrahydro-naphthalene-2-carboxylic Acid | HCID 19069973 | 92,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05725798 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-7d2c74c555f047899e0fbc54d1163d31 |
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| Quellennotiz | uspto-grants-1998_03 |
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