Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | HCID 24707301 | HCID 24707301 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59402770 | HCID 59402770 | 49.2% |
Reaction Steps
To the solution of 2-Benzyloxy-thioacetamide (3.0 g, 16.57 mmol) in 3 ml of DMF was added 2-Bromo-1-(4-chloro-phenyl)-ethanone (3.0 g, 12.87 mmol). The reaction mixture was heated at 130° C. for 24 h under nitrogen atmosphere. After the completion of the reaction mixture (TLC monitoring), water (25 mL) was added and extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (230-400 M, 2% EtOAc-Hexane) to get the desired product (2.0 g, 49%). The corresponding cyano derivative was also prepared by the same general method.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865736B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-23174da9da0c49ccbedf34c8e0e82416 |
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| Source note | uspto-grants-2014_10 |
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