Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylbenzene | HCID 7500 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 2-Phenyl-1-propanol | HCID 14295 | — |
| Reactant | Tin atom | HCID 5352426 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Propylene Carbonate | HCID 7924 | — |
| Product | Benzenepropanol | HCID 31234 | — |
Reaction Steps
Tin methylate Sn(OCH3)2 is produced according to the method disclosed by J. Morrison and H. Haendler, 29 J. Inorg. Nucl. Chem., 393-400 (1967). A catalytic system comprising 66.4 mg of LPtCl2 (L being the same ligand as in example 12) and 15.7 mg tin methylate in a solvent consisting of a mixture of 15 cm3 benzene and 10 cm3 propylene carbonate is introduced under nitrogen into a 100 cm3 stainless steel autoclave reactor equipped with a bar magnet stirring system. Then, 1.23 g styrene is added. The reactor is heated to a temperature of 90° C. and then filled with an equimolar mixture of carbon monoxide and hydrogen (synthesis gas). The resulting mixture is stirred and the reaction continued at 90° C. under a pressure of 100 bars for a time (T) expressed in hours. A mixture of ethylbenzene, 2-phenylpropanol and 3-phenylpropanol is obtained with a degree of conversion (DC). The proportion by weight of ethylbenzene (EB) and the molar ratio (n/b) are determined as above. The results are reported in Table V below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04923840 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-8535f1fc5187404783d2713abbb2405a |
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| Source note | uspto-grants-1990_05 |
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