HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-((3,5-Dichloro-2-cyanobenzyl)oxy)ethyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Glycol monoacetate | HCID 10960 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Bromomethyl)-4,6-dichlorobenzonitrile | HCID 89704997 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-((3,5-Dichloro-2-cyanobenzyl)oxy)ethyl acetate | HCID 89704826 | — |
Reaction Steps
To a solution of 2-(bromomethyl)-4,6-dichlorobenzonitrile (1.3 mmol) (A.2.5.1) and 2-hydroxyethyl acetate (1.43 mmol) in 7 mL THF was added NaH (1.95 mmol, 60% suspension in oil). The reaction mixture was stirred at RT overnight and then poured into a 1M HCl solution. The mixture was extracted twice with EtOAc. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification with CC (KP-SIL™ from Biotage) using Hept to Hept/EtOAc (75/25) gives the desired compound as orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409917B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-e53df6c0f1f04847b3fac0a09a35f66a |
| Source note | uspto-grants-2016_08 |