HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417887Generated: November 3, 2026
Bromine → 2-Acetoxy-5-(2-bromoacetyl)benzyl acetate
https://huagongshe.com/reaction/2417887
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethanone, 1-[4-(acetyloxy)-3-[(acetyloxy)methyl]phenyl]- | HCID 154871 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Acetoxy-5-(2-bromoacetyl)benzyl acetate | HCID 11278896 | 69.1% |
Reaction Steps
A solution of bromine (7.1 g.) in chloroform (20 ml.) was added dropwise to a stirred solution of 3'-acetoxymethyl-4'-acetoxyacetophenone (11.0 g.) in chloroform (150 ml.) at room temperature. After completion of the addition, the solution was washed with water (2×150 ml.) and brine (100 ml.). The organic phase was dried (MgSO4), filtered and evaporated to give 3'-acetoxymethyl-4'-acetoxy-2-bromoacetophenone (10.0 g.) which was judged to be sufficiently pure by IR and TLC [SiO2 ; 1:1 v/v EtOAc/petrol (60°-80° C.)] for use without further purification or characterisation. A solution of 3'-acetoxymethyl-4'-acetoxy-2-bromoacetophenone (10.0 g.) in dimethylsulphoxide (150 ml.) was stirred at room temperature for 48 hours. The solution was then poured into ice-water (500 ml.) and extracted with ethyl acetate (3×200 ml.). The organic layers were combined, dried (MgSO4) filtered. The solvent was removed by evaporation to give 3'-acetoxymethyl- 4'-acetoxy-phenylglyoxal hydrate as a yellow oil (6.5 g. 81%). The glyoxal derivative had a satisfactory IR spectrum and was judged pure by TLC (SiO2 : EtOAc) and was therefore used without full characterisation or isolation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04470997 |
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| Source dataset | uspto-grants-1984_09 |
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| ORD ID | ord-f50f3c7ba5e9423b86aaad909e81f20f |
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| Source note | uspto-grants-1984_09 |
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