HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → 3-Ethyl-4-isopropoxy-benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Ethyl-4-hydroxybenzaldehyde | HCID 22038713 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Ethyl-4-isopropoxy-benzaldehyde | HCID 22039201 | — |
Reaction Steps
A mixture of the 3-ethyl-4-hydroxy-benzaldehyde (7.8 g, 51.9 mmol) obtained in Example 179.1, K2CO3 (10.8 g, 78 mmol) and isopropyl iodide (7.86 ml, 78 mmol) was heated in DMF (65 ml) for 3 h. to 80° C. and subsequently stirred for 12 h. at room temperature. The mixture was poured into ice-cold 0.5M HCl and extracted with diethyl ether. The organic phase was washed with NaCl solution, dried, filtered and concentrated. The residue was purified by chromatography (SiO2, hexane/EtOAc 4:1). 3-Ethyl-4-isopropoxy-benzaldehyde was obtained as an orange oil (6.12 g, 61%); MS: 192 ([M]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476264B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-6cc2ade04ebc490db78b792344d6485e |
| Source note | uspto-grants-2002_11 |