HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786973Generated: October 29, 2026
3-Chloro-4-(3-fluorobenzyloxy)aniline → HCID 86626251, compound
https://huagongshe.com/reaction/1786973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-4-(3-fluorobenzyloxy)aniline | HCID 7059263 | — |
| Reactant | HCID 86084730 | HCID 86084730 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 86626251 | HCID 86626251 | 73.9% |
Reaction Steps
To a solution of ethyl (4-chloro-5H-pyrrolo[3,2-d]pyrimidin-5-yl)acetate (530 mg) in isopropyl alcohol (4.0 mL) was added 3-chloro-4-[(3-fluorobenzyl)oxy]aniline (695 mg), and the mixture was stirred in an oil bath at a temperature of 100° C. for 2.5 hrs. The reaction mixture was allowed to cool to room temperature, diluted with 5% aqueous sodium hydrogen carbonate solution (25 mL), and extracted with ethyl acetate (30 mL×3). The organic layer washed successively with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to basic silica gel chromatography (eluent:hexane/ethyl acetate=95/5→20/80). The object fraction was concentrated under reduced pressure and dried to give the title compound (743 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07507740B2 |
|---|
| Source dataset | uspto-grants-2009_03 |
|---|
| ORD ID | ord-9f3987e234d94d20946c7cb74fdab4d9 |
|---|
| Source note | uspto-grants-2009_03 |
|---|