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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330268Erstellt: 25. Oktober 2026

1-Chloro-3,4-dihydronaphthalene-2-carboxaldehyde → (1-Chloro-3,4-dihydronaphthalen-2-yl)methanol

https://huagongshe.com/reaction/330268

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-3,4-dihydronaphthalene-2-carboxaldehydeHCID 76752—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(1-Chloro-3,4-dihydronaphthalen-2-yl)methanolHCID 14819335102,2%

Reaktionsschritte

To a mixture of sodium borohydride (2.83 g, 0.075 mol) in methanol (150 mL) at 0° C., was added dropwise a solution of 1-chloro-2-formyl-3,4-dihydronaphthalene (9.59 g, 0.05 mol) in dry THF (150 mL). The reaction was stirred at room temperature for 1 hour, carbon dioxide was cautiously bubbled through the reaction mixture for 15 minutes, and the resulting mixture was concentrated under reduced pressure. The residue was diluted with water (150 mL), extracted with ether (3×150 mL), dried (MgSO4) and concentrated to give 9.95 g (102%) of product as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04895860
Quelldatensatzuspto-grants-1990_01
ORD IDord-a203c78374d04dca998de492e3dae3ff
Quellennotizuspto-grants-1990_01