HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2-Methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 2-Phenylethanol | HCID 6054 | — |
| Reactant | 1-Phenylethanol | HCID 7409 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methylbenzaldehyde | HCID 10722 | 385% |
Reaction Steps
The experimental procedure was substantially the same as in Example excepting replacement of the benzene as the starting hydrocarbon compound with the same volume of toluene. The reaction mixture after completion of the reaction contained position isomers of methylbenzyl alcohol in a total molar yield of 6332% based on the amount of the rhodium complex used as the catalyst including o-, m- and p-methylbenzyl alcohols in a proportion of 3:60:37. 2-phenylethyl alcohol was not detected in the reaction mixture. Tolualdehyde was produced in a molar yield of 385% as a total value for the o-, m and p-isomers relative to the rhodium complex used as the catalyst.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05104504 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-17637f4bc4e54001898f82347923678a |
| Source note | uspto-grants-1992_04 |