HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylbenzyl alcohol → 2-Methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylbenzyl alcohol | HCID 6994 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 3-amino-N-hydroxyphthalimide | HCID 10888472 | — |
| Product | 2-Methylbenzaldehyde | HCID 10722 | 30% |
Reaction Steps
170 mg (1.60 mmol) of o-xylene were reacted analogously to Example 1 in the presence of 32.1 mg (0.180 mmol) of 3-amino-N-hydroxyphthalimide. After a reaction time of 4 hours and 18 hours, a further 32.1 mg (0.180 mmol) of 3-amino-N-hydroxyphthalimide were added in each case, and, after a total of 30 hours, the reaction solution was extracted with chloroform and examined by NMR spectroscopy. Yield 30% of 2-methylbenzaldehyde and 7% of 2-methylbenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297403B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-1891e06b840d49d48dfd203a556d703d |
| Source note | uspto-grants-2001_10 |