Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (4-Methoxyphenyl)(3-methylphenyl)methanone | HCID 12469466 | — |
| Solvent | 1,2-Dibromoethane | HCID 7839 | — |
| Product | HCID 54452167 | HCID 54452167 | 60.8% |
Reaction Steps
A solution of the benzophenone (17.5 g, 77.4 mmole) of Step A in ethylene bromide (26.5 mL) (containing a small amount of benzoyl peroxide) is heated at reflux. A solution of bromine (12.7 g, 79.6 mmole) in ethylene bromide (15 mL) is added dropwise over 30 minutes while the mixture is irradiated with a Photolamp (300 W). Reflux is continued for 17 hours (TLC, 9:1 petrolether-ethylacetate, traces of starting material still present). The solvent is removed in vacuo and the residue (brown oil, 39.22 g) is purified by flask chromatography (on silica Merck-60, preabsorbed in dichloromethane, eluted with 9:1 petrolether-ethyl acetate) to give unreacted starting material (2.59 g, ca.. 15%) along with the desired product (14.36 g, 61% or 71.5% based on recovered unreacted starting material) and some mixed fractions (ca. 5.20 g). The light yellow solid melts at 58°-61 ° C. and it is used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05364944 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-fff8af551f3a4b94a16e774522e12941 |
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| Source note | uspto-grants-1994_11 |
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