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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486401Generated: October 30, 2026

Triethylamine → 2-Bromo-1-(6-bromonaphthalen-2-yl)ethanone

https://huagongshe.com/reaction/1486401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiethylphosphiteHCID 3780918—
Reactant2,2-Dibromo-1-(6-bromonaphthalen-2-yl)ethanoneHCID 86669978—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-1-(6-bromonaphthalen-2-yl)ethanoneHCID 1269889897%

Reaction Steps

2,2-dibromo-1-(6-bromonaphthalen-2-yl)ethanone (90.0 g, 221 mmol, 1.00) was dissolved in tetrahydrofurane (800 mL), triethylamine (27.67 mL, 199 mmol, 0.9 equiv.) was added followed by diethyl phosphite (45.8 g, 332 mmol, 1.50 equiv.). The reaction mixture was stirred overnight. The reaction mixture was filtrated and the solvent was removed in vacuum. The obtained residue was dissolved in ethyl acetate (1.2 L) and washed with water. The organic layer was separated, dried over sodium sulphate, filtrated and concentrated to yield crude 2-bromo-1-(6-bromonaphthalen-2-yl)ethanone (70.3 g). Recrystallization from acetonitrile gave 30 g (first batch) and 6.5 g (second batch) of 2-bromo-1-(6-bromonaphthalen-2-yl)ethanone (50%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09427428B2
Source datasetuspto-grants-2016_08
ORD IDord-f8ee39b9bb664b66b4f71993f6069e75
Source noteuspto-grants-2016_08