HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → HCID 22107237, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- | HCID 112414 | — |
| Reactant | Sodium o-chlorobenzoate | HCID 23663665 | — |
| Reactant | Sodium 2-cyclohexylphenolate | HCID 23684558 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 22107237 | HCID 22107237 | 68% |
Reaction Steps
A mixture of 21.4 g (0.12 mol) of sodium 2-chlorobenzoate, 26.1 g (0.132 mol) of sodium 2-cyclohexylphenolate, 4.95 g (0.05 mol) of copper(I) chloride and 16.17 g (0.05 mol) of tris[2-(2-methoxyethoxy)-ethyl]amine (TDA) in 1.5 1 of diethylene glycol dimethyl ether ("diglyme") is kept at 140° C. for 8 hours. The solvent is then concentrated on a vacuum rotary evaporator and the residue is diluted with water and acidified with concentrated hydrochloric acid. The product is extracted with ethyl acetate. The organic phases are washed with water, combined, dried over sodium sulfate and concentrated on a vacuum rotary evaporator. 22.2 g (68%) of 2-(2-cyclohexylphenoxy)benzoic acid, melting point 109°-123° C., result as a beige powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05710198 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-c6a1053f130b483b8d7e9bf6c035a9d1 |
| Source note | uspto-grants-1998_01 |