HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Acetoxy-1-(3-chlorophenyl)-2-(2-tertbutoxyethoxy)ethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-(3-Chlorophenyl)-2-(2-tertbutoxyethoxy)ethanol | HCID 53835502 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetoxy-1-(3-chlorophenyl)-2-(2-tertbutoxyethoxy)ethane | HCID 53824717 | 93.7% |
Reaction Steps
37.0 g of 1-(3-chlorophenyl)-2-(2-tert-butoxyethoxy)ethanol was dissolved in 70 ml of methylene chloride. To the solution were added 12.9 g of pyridine and 16.6 g of acetic anhydride. The resulting mixture was stirred for 24 hours at room temperature. The reaction mixture was added to a mixture of 150 ml of ice water and 100 ml of methylene chloride. The resulting mixture was adjusted to pH 2 with 6N hydrochloric acid. The organic layer was separated, washed with a saturatred aqueous sodium hydrogencarbonate solution and water in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain 40.0 g of oily 1-acetoxy-1-(3-chlorophenyl)-2-(2-tert-butoxyethoxy)ethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719150 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-98df1ad371fb46ad9940795d97b6cecc |
| Source note | uspto-grants-1998_02 |