HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721222Generated: October 30, 2026
2,6-Dimethoxyphenol → HCID 21889944, compound
https://huagongshe.com/reaction/721222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dimethoxyphenol | HCID 7041 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-[(6,7-Dimethoxyquinolin-4-yl)oxy]aniline | HCID 11594543 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 21889944 | HCID 21889944 | 99.5% |
Reaction Steps
4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (50 mg) was added to toluene (5 ml), and triethylamine (0.5 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (77 mg) in methylene chloride was then added thereto, and the mixture was heated under reflux for 10 min. Next, 2,6-dimethoxyphenol (40 mg) was added thereto, and the mixture was further stirred with heating under reflux for 3 hr. A saturated aqueous sodium bicarbonate solution was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution, water, and saturated brine in that order. The extract was dried over sodium sulfate and was then concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (80 mg, yield 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07135466B2 |
|---|
| Source dataset | uspto-grants-2006_11 |
|---|
| ORD ID | ord-0439c09061d5436a865a922a76f73e76 |
|---|
| Source note | uspto-grants-2006_11 |
|---|