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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720017Generated: October 31, 2026

Bromoacetyl bromide → 7-Bromoacetyl-9,9-diethyl-2-diphenylaminofluorene

https://huagongshe.com/reaction/720017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant9,9-Diethyl-2-diphenylaminofluoreneHCID 21902184—
Solvent1,2-DichloroethaneHCID 11—
Product7-Bromoacetyl-9,9-diethyl-2-diphenylaminofluoreneHCID 2190218266.3%

Reaction Steps

To a suspension of aluminium chloride (0.375 g, 2.82 mmol) in 1,2-dichloroethane (15 ml) at 0° C. was added a solution of 2-diphenylamino-9,9-diethylfluorene (1.0 g, 2.57 mmol) in 1,2-dichloroethane (15 ml). Bromoacetyl bromide (0.269 ml, 3.08 mmol) was added over a period of 10 min to maintain a steady reaction temperature between 0–10° C. under an ice-bath. At the end of addition, the mixture was warmed to ambient temperature, stirred for another 4 h, and quenched by a slow addition of water (50 ml) to maintain the mixture temperature below 45° C. Organic layer was washed subsequently with dil. HCl (1.0 N, 50 ml) and water (50 ml, twice). It was concentrated in vacuuo to give crystalline yellow solids. These crude products were purified by column chromatography (silica gel, hexane-toluene/3:2 as eluent, Rf=0.3 on thin layer chromatography using the same solvent mixture as eluent) to afford 7-bromoacetyl-9,9-diethyl-2-diphenylaminofluorene (0.87 g) as yellow crystalline solids in a yield of 66%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132572B2
Source datasetuspto-grants-2006_11
ORD IDord-e691b07cf0f64d4dbd59149634668713
Source noteuspto-grants-2006_11