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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55756Generated: October 27, 2026

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

https://huagongshe.com/reaction/55756

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 numberUS09433609B2
Source datasetuspto-grants-2016_09
ORD IDord-7e3b810e270a4f29aefca102ad63e1a8
Source noteuspto-grants-2016_09