HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 66778911, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Chloro-3-methyl-1-benzofuran-2-carbaldehyde | HCID 4736982 | — |
| Reactant | HCID 178419651 | HCID 178419651 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66778911 | HCID 66778911 | 60% |
Reaction Steps
To a solution (10 mL) of 5-chloro-3-methyl-1-benzofuran-2-carbaldehyde (600 mg) synthesized above in tetrahydrofuran was added a 1.0M solution (4.62 mL) of cyclohexylmagnesium bromide in tetrahydrofuran at 0° C., and the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (15% ethyl acetate/hexane) to give the title object compound (518 mg, 60%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-697f5aa0ca3b455b9a98e36de6324088 |
| Source note | uspto-grants-2013_05 |