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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131645Generated: October 26, 2026

Dimethylformamide → 5-(Benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-one

https://huagongshe.com/reaction/131645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
Reactant5-Hydroxy-1-tetraloneHCID 119921—
ReactantHCID 178418922HCID 178418922—
SolventWaterHCID 962—
Product5-(Benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10586915—

Reaction Steps

3.1 g of t-butoxypotassium was added under ice cooling and nitrogen replacement to a 50 mL dimethylformamide solution of 4.0 g of 5-hydroxytetralone, and the system was stirred for 15 minutes at the same temperature, after which 3.2 mL of benzyl bromide was added, and the system was stirred for 2 hours at the same temperature. After the reaction, water was added, extraction was performed with ethyl acetate, and the organic layer was washed with saturated brine and dried with magnesium sulfate, then subjected to reduced-pressure solvent distillation, and the residue was refined by silica gel column chromatography (20% ethyl acetate/hexane) to obtain 6.3 g of 5-benzyloxytetralone (compound 2-7 in Table 3-1) in the form of a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384974B2
Source datasetuspto-grants-2008_06
ORD IDord-9f1f1b83711341b69f8cd650bf3ddf8d
Source noteuspto-grants-2008_06