HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5-Chloro-2-nitrobenzaldehyde diethyacetal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 5-Chloro-2-nitrobenzaldehyde | HCID 81123 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Chloro-2-nitrobenzaldehyde diethyacetal | HCID 13236299 | 93% |
Reaction Steps
A mixture of 5-chloro-2-nitrobenzaldehyde (5.0 g), toluene (50 ml), p-toluenesulfonic acid monohydrate (25 mg) was heated under stirring for 2 hours by dehydrating water which was formed in the course of reaction. The solvent was distilled under reduced pressure and the residue was column chromatographed (hexane/ethyl acetate: 8/1) to give 6.5 g of the pure title compound (93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05171851 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-762d8d9f3b824d3d867bce3db879c174 |
| Source note | uspto-grants-1992_12 |