Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl phenyl sulfone | HCID 18369 | — |
| Reactant | 2-Bromo-1-(3-bromophenyl)ethan-1-one | HCID 519585 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14580198 | HCID 14580198 | 20% |
Reaction Steps
In a manner identical with Example 57, 2,3'-dibromoacetophenone (7.8 g, 0.028 mole) is treated with 1 equivalent of the magnesium anion of methyl phenyl sulphone in THF at -70° C. The mixture is stirred for 2 h at -70° C., acetic acid (7 cc) is then added and the mixture is poured into water (100 g). It is reextracted with ether (3×100 cc), is washed with brine (2×100 cc) and is dried over MgSO4. The crude is precipitated with ether (50 cc) with warming and recrystallized from isopropyl ether to give white crystals of 1-bromo-2-[3'-bromophenyl]-3-phenylsulphonyl-2-propanol (2.4 g, 20%). Mp=132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05100460 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-44f70c0a0ced4c0b87ca341a6b721166 |
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| Source note | uspto-grants-1992_03 |
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