HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006449Generated: October 29, 2026
Bromoacetyl bromide → Ethyl 2-[4-(2-bromoacetyl)-3-chlorophenoxy]-2-methylpropionate
https://huagongshe.com/reaction/1006449
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Ethyl 2-(3-chlorophenoxy)-2-methylpropanoate | HCID 1531499 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Ethyl 2-[4-(2-bromoacetyl)-3-chlorophenoxy]-2-methylpropionate | HCID 15453491 | — |
Reaction Steps
To a stirred suspension of aluminum chloride (1.8 g) in 1,2-dichloroethane (25 ml) was added bromoacetyl bromide (400 μl) under ice-cooling, and the mixture was stirred for 30 minutes. To the stirred mixture was added dropwise a solution of ethyl 2-(3-chlorophenoxy)-2-methylpropionate (1.1 g) in 1,2-dichloroethane (5 ml) under ice-cooling, and the mixture was stirred for 3 hours at 60° C. The reaction mixture was poured into ice-water and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. Purification of the residue by flash column chromatography on silica gel (eluent: hexane/ethyl acetate=10/1) gave ethyl 2-[4-(2-bromoacetyl)-3-chlorophenoxy]-2-methylpropionate (204 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790865B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-3c9245290983469ab1d2d5c1f8dbf793 |
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| Source note | uspto-grants-2004_09 |
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