HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614513Generated: October 29, 2026
Hydrofluoric Acid → 4-Fluoro-3-methoxyaniline
https://huagongshe.com/reaction/614513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | Benzene, 1-azido-3-methoxy- | HCID 542844 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Fluoro-3-methoxyaniline | HCID 2774533 | — |
Reaction Steps
A solution of 10.73g. (0.07 mole) of 3-methoxyphenylazide in 100 ml. of hexane was added to 20 ml. of concentrated hydrofluoric acid and the reaction mixture, contained in a bomb, was aged for 10 hours at room temperature with agitation. The reaction mixture was then cooled, vented, and poured from the bomb. The bomb was then rinsed with 50 ml. of water, followed by 20 ml. of dichloromethane. The reaction mixture poured from the bomb was blown down under nitrogen, and then combined with the bomb rinsings, and this mixture was cooled and brought to a pH of about 12 with KOH pellets. The mixture was extracted three times with 50 ml. of dichloromethane per extraction, and the combined extracts were dried over MgSO4 and concentrated to 7.31g. (53%) of a dark oil. An aliquot of this product was distilled under reduced pressure to obtain a pale yellow oil with a b.p. of 150°-152° C. at 50 mm. Hg. Structure of the final product as 3-methoxy-4-fluoroaniline was confirmed by mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04145364 |
|---|
| Source dataset | uspto-grants-1979_03 |
|---|
| ORD ID | ord-711f4c76fd794b3a97bab1f5cb8882a5 |
|---|
| Source note | uspto-grants-1979_03 |
|---|