HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Chlorophenoxy)ethylamine → Ethyl{[({2-[(4-chlorophenyl)oxy]ethyl}-amino)carbonyl]oxy}acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Chlorophenoxy)ethylamine | HCID 2794191 | — |
| Reactant | Ethyl [(phenoxycarbonyl)oxy]acetate | HCID 12094709 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl{[({2-[(4-chlorophenyl)oxy]ethyl}-amino)carbonyl]oxy}acetate | HCID 91288841 | — |
Reaction Steps
A solution of 0.6 g (3.5 mmol) of [(4-chloro-phenyl)oxy]ethylamine (Chim. Ther. 1973, 8, 259-270) and 1.3 g (5.8 mmol) of ethyl [(phenyloxy-carbonyl)oxy]acetate, prepared in Step 1.1., in 30 ml of toluene is heated at 60° C. overnight. It is evaporated to dryness and the product is purified by chromatography on silica gel, eluting with a 30/70 mixture of ethyl acetate and cyclohexane. This gives 0.7 g of oily product, containing ˜10% of cyclized oxazolidine dione product, used as it is in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07439257B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-ed6b8fecc7394dd98990156476ad2dc3 |
| Source note | uspto-grants-2008_10 |