HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1-(Dimethoxymethyl)-2-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(Dimethoxymethyl)-2-fluorobenzene | HCID 11426732 | — |
Reaction Steps
A mixture of 12.2 g of 2-fluorobenzaldehyde, 15 ml of 2,2-dimethoxypropane and 0.1 g of 4-toluenesulphonic acid was stirred at room temperature. After 24 hours, diethyl ether was added and the resultant solution washed with saturated sodium bicarbonate solution. Drying and evaporation of the organic phase gave the crude acetal. Distillation under vacuum at 90°-95° C./0.08 mm yielded the title compound as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04629737 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-97a43d6db0e847688358fe9bece11458 |
| Source note | uspto-grants-1986_12 |