HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-(Benzyloxy)-3-(tert-butyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Benzyloxy-2-tert-butyl-4-methyl-benzene | HCID 50886343 | — |
| Product | 4-(Benzyloxy)-3-(tert-butyl)benzaldehyde | HCID 14772634 | — |
Reaction Steps
A solution of 6.985 g 1-benzyloxy-2-tert-butyl-4-methyl-benzene (27 mmol) and 115 g ammoniumcer (IV)-nitrate in 1000 ml acetic acid (50% v/v) was stirred at 90° C. for one hour. After cooling down to RT, the reaction mixture was extracted with AcOEt/heptane 1:9, dried over magnesium sulfate, filtered off and concentrated under vacuo. The residue was purified by flash column chromatography (heptane/AcOEt 95/5 to 90/10) to give 3.48 g of an orange solid. MS (ISP) 269.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745477B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-ba32652dd21c4f8c82cf31c059f4cbec |
| Source note | uspto-grants-2010_06 |