HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Chloro-1,1-diethoxy-2-methylpropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Propanal, 2-chloro-2-methyl- | HCID 13513 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Catalyst | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-1,1-diethoxy-2-methylpropane | HCID 15186227 | 68.2% |
Reaction Steps
To a mixture of 45 g (0.424 mol) of 2-chloro-2-methylpropanal, 99.6 ml (1.69 mol) of ethanol, 81.6 g (0.55 mol) of triethylorthoformate in 100 ml of methylene chloride was added 800 mg (4.2 mmol) of p-toluenesulfonic acid and the mixture was stirred at room temperature. After adding 2 g of potassium carbonate to the above mixture, the reaction mixture was stirred (2 min.), and filtered. The filtrate was concentrated (80° C.) to remove methylene chloride and the residue was distilled (2×) to afford 52 g (68.2%) of 2-chloro-2-methylpropanal diethyl acetal, b.p. 55°-65° C./25 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380729 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-894c34e1de6e40329269814b41dca283 |
| Source note | uspto-grants-1995_01 |