HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 1-(2'-(Benzyloxy)-3'-phenybiphenyl-3-yl)-1-(2-methoxyphenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(2'-(Benzyloxy)-3'-phenylbiphenyl-3-yl)ethanone | HCID 58238595 | — |
| Reactant | HCID 178489560 | HCID 178489560 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2'-(Benzyloxy)-3'-phenybiphenyl-3-yl)-1-(2-methoxyphenyl)ethanol | HCID 58238603 | — |
Reaction Steps
A solution of 32 (1.5 g, 3.96 mmol) in anhydrous tetrahydrofuran (16 mL) was stirred under nitrogen at room temperature and 1M ortho-methoxyphenyl magnesium bromide in tetrahydrofuran (6 mL, 1.5 equiv.) was slowly added. Stirring was continued at room temperature for 30 min and at 60° C. for 3 hr. After cooling, the reaction mixture was poured on saturated ammonium chloride (100 mL) and extracted with ethyl acetate (150 mL). The organic extract was washed with water (2×100 mL), dried over sodium sulfate and filtered. The solvent was removed in a rotary evaporator and the crude 33 thus obtained was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541522B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-28d11bf4acba41d78da6c3b17b37123a |
| Source note | uspto-grants-2013_09 |