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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375248Generated: November 1, 2026

7-Bromo-1,2,3,4-tetrahydronaphthalen-1-one → 7-Bromo-1,2,3,4-tetrahydronaphthalen-1-ol

https://huagongshe.com/reaction/2375248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Bromo-1,2,3,4-tetrahydronaphthalen-1-oneHCID 252731—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product7-Bromo-1,2,3,4-tetrahydronaphthalen-1-olHCID 12694919—

Reaction Steps

To 9.5 g of 7-bromo-3,4-dihydronaphthalen-1(2H)-one (42 mmol), prepared according to the method described in Synth. Comm. 1994, 2777, dissolved in 100 ml of ethanol, there are added, at 0° C. and in two portions,0.8 g of sodium borohydride (21 mmol). The reaction mixture is then allowed to come back up to ambient temperature over 30 minutes, and then the ethanol is evaporated off. The residue is taken up in 100 ml of toluene and 100 ml of water. After separation, the aqueous phase is extracted with 50 ml of toluene. The toluene phases are combined, washed with a saturated aqueous solution of sodium chloride and are then evaporated to yield 7-bromo-1,2,3,4-tetrahydronaphth-1-ol in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465733B2
Source datasetuspto-grants-2008_12
ORD IDord-802de41f3e254972a11b4a72af68f8c8
Source noteuspto-grants-2008_12