HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → (4-(Allyloxy)-5-bromo-2-chlorophenyl)(4-ethylphenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(Allyloxy)-5-bromo-2-chloro-N-methoxy-N-methylbenzamide | HCID 86714021 | — |
| Reactant | HCID 178436501 | HCID 178436501 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-(Allyloxy)-5-bromo-2-chlorophenyl)(4-ethylphenyl)methanone | HCID 86714031 | 84.5% |
Reaction Steps
To solution of Weinreb amide 22 (4.5 g, 13.4 mmol) in THF (100 mL) was added 4-ethylphenylmagnesium bromide (0.5 M in THF, 50.8 mL, 26.9 mmol) at 0° C. The reaction mixture was warmed up to r.t. slowly and stirred at r.t. for 15 hours. To the reaction mixture was added aqueous saturated NH4Cl solution (100 mL). The mixture was extracted with EtOAc (100 mL). The organic layer was dried over MgSO4, filtered and concentrated in vacuo. The residue was triturated with hexane (100 mL) and stirred at r.t. for 30 min. The solid was precipitated, filtered, washed with hexane (50 mL) and dried under high vacuum to obtain the title product (4.30 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09371303B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-41966a268cd4430d85dfd29979547c7a |
| Source note | uspto-grants-2016_06 |