HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038348Generated: October 31, 2026
Hydrochloric Acid → 1-Bromo-4-cyano-3-methoxy-5-(4-ethyl-benzyl)-benzene
https://huagongshe.com/reaction/1038348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Bromo-2,6-difluorobenzonitrile | HCID 2756916 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Ethyl 2-(4-ethylphenyl)acetate | HCID 53419404 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-Bromo-4-cyano-3-methoxy-5-(4-ethyl-benzyl)-benzene | HCID 58385818 | — |
Reaction Steps
KOtBu (11.8 g) is added to a flask charged with a stir bar and dry NMP (40 mL) and chilled to −10° C. under argon atmosphere. A solution of ethyl (4-ethyl-phenyl)-acetate (10.1 g) and 1-bromo-4-cyano-3,5-difluoro-benzene (11.5 g) in NMP (40 mL) is added at such a rate that the reaction temperature maintains below 10° C. After stirring for 1 hour at room temperature, methanol (50 mL) and 1 M aqueous sodium hydroxide solution (39 mL) are added and the resulting mixture is stirred overnight at 100° C. Then, 4 M aqueous hydrochloric acid (100 mL) is added and the mixture is stirred for another h at 100° C. The methanol fraction is evaporated, water (200 mL) is added to the residue and the resulting mixture is extracted with ethyl acetate. The combined organic extracts are washed twice with water, twice with brine and dried (MgSO4). The solvent is evaporated and the residue is washed with methanol. The insoluble residue is separated by filtration and dried to give the white product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08551957B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-a8f6ea36c3b442f6849ce241222ea0ea |
|---|
| Source note | uspto-grants-2013_10 |
|---|