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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388588Generated: November 2, 2026

Sodium borohydride → 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/1388588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-oneHCID 5044385—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-olHCID 1969948880%

Reaction Steps

Sodium borohydride (1.67 g) was added in portions to a solution of 6-fluoro-2-tetralone (6.56 g) in dry ethanol (30 ml) with stirring, keeping the temperature below 25° C. The mixture was then stirred at room temperature for 3 hours. The mixture was then diluted with a little ethyl acetate and concentrated to an oily residue. Dilute sulphuric acid was added dropwise until effervescence no longer occurred. The mixture was extracted with ether and the extract washed, dried, and concentrated to give an oil. This was distilled (b.p. 75-77/0.1 Torr) to give 6-fluorotetralin-2-ol (5.31 g) containing a trace of the tetralone starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431834
Source datasetuspto-grants-1984_02
ORD IDord-80fcd6266e90474a9d86e62215b9613f
Source noteuspto-grants-1984_02