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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653745Generated: October 31, 2026

Oxalyl chloride → 5-Bromo-1,2,3,4-tetrahydronaphthalen-1-one

https://huagongshe.com/reaction/653745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4-(2-Bromophenyl)butanoic acidHCID 13330230—
SolventBenzeneHCID 241—
Product5-Bromo-1,2,3,4-tetrahydronaphthalen-1-oneHCID 1088957292%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a benzene solution (60 ml) of 4-(o-bromophenyl) butyric acid (5 g) was added oxalyl chloride (3.6 ml) and the reaction refluxed for 11/2 hrs. The solution was evaporated to dryness, the residue was dissolved in CH2Cl2 (50 ml) then cooled to 0° C., followed by the addition of AlCl3 (3.1 g). The mixture was stirred at 0° C. warming to room temperature overnight. The reaction was poured onto ice, then extracted with CH2Cl2. The organic layer was separated, washed with 1N NaOH, then brine, separated, dried (MgSO4), filtered and evaporated affording the desired product (4.26 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05128362
Source datasetuspto-grants-1992_07
ORD IDord-a533272a5fe5427ebb632e7b35cfc897
Source noteuspto-grants-1992_07