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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 9,9-Diethyl-2-diphenylaminofluorene | HCID 21902184 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 7-Bromoacetyl-9,9-diethyl-2-diphenylaminofluorene | HCID 21902182 | 66.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132572B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-e691b07cf0f64d4dbd59149634668713 |
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| Source note | uspto-grants-2006_11 |
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