Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | HCID 53893725 | HCID 53893725 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14403425 | HCID 14403425 | 90% |
Reaction Steps
460 mg (0.5 mmol) of tris-triphenylphosphinerhodium chloride (=1 mol-%, with respect to the reaction component) are added to a 100 ml autoclave. After purging with nitrogen, an air-free solution of 15.7 g (0.05 mol) of 4-chlorophenyl-ethenyl 1-phenylmercapto-cyclopropyl ketone in 40 ml of toluene is added and the mixture is heated to 50° C. under a hydrogen pressure of 30 bar. The hydrogen pressure is held between 40 and 50 bar until gas uptake has ended. The mixture is then reacted for a further hour. For working up, the solvent is stripped off under reduced pressure and the residue remaining is purified on silica gel using dichloromethane as eluant. 14.2 g (90% of theory) of 4-chlorophenylethyl 1-phenylmercaptocyclopropyl ketone are obtained in the form of an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983208 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-d5fa91bcbdd94144abddbb294a12b0a2 |
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| Source note | uspto-grants-1991_01 |
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