HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1047349Erstellt: 25. Oktober 2026
Sodium Hydroxide → 7-Chloro-1,6-dihydroxynaphthalene
https://huagongshe.com/reaction/1047349
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Boron tribromide | HCID 25134 | — |
| Edukt | 7-Chloro-1,6-dimethoxynaphthalene | HCID 58705169 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 7-Chloro-1,6-dihydroxynaphthalene | HCID 57892884 | 88% |
Reaktionsschritte
A 50 ml round bottom flask equipped with magnetic stirring bar was charged with solution of compound 47 (2.0 g, 9.0 mmol) in anhydrous CH2Cl2 (20 ml). Flask was filled in with argon atmosphere and BBr3 (9.0 g, 3.39 ml, 36.0 mmol) was added through a syringe over 5 min. Resultant mixture was magnetically stirred overnight at room temperature. Reaction mixture was carefully poured into ice-water mixture (30 g), diluted with CH2Cl2 and neutralized by addition of 2% NaOH (pH˜6-7). Organic phase was separated, washed with NaHCO3 (2×10 ml) and NaCl (20 ml) solutions, dried over MgSO4 and concentrated in vacuum to give desired product 48 (1.54 g, 7.9 mmol, 88% yield) as fluffy off-white solid. 1H NMR (DMSO-d6): δ 10.45 (s, 1H), 10.13 (s, 1H), 8.04 (s, 1H), 7.23-7.10 (m, 3H), 6.67 (d, J=7.3 Hz, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08569516B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-40ac595e22814f9fb69d30ed5cfd65a4 |
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| Quellennotiz | uspto-grants-2013_10 |
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