HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 5-[[6-([1,1'-Biphenyl]-4-yloxy)hexyl]oxy]-2-(phenylmethoxy)benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-[[6-([1,1'-Biphenyl]-4-yloxy) hexyl]oxy]-2-hydroxybenzoic acid methyl ester | HCID 54513465 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[[6-([1,1'-Biphenyl]-4-yloxy)hexyl]oxy]-2-(phenylmethoxy)benzoic acid methyl ester | HCID 54022805 | 89% |
Reaction Steps
A mixture of 1.4 g (3.3 mmol) of 5-[[6-([1,1'-biphenyl]-4-yloxy) hexyl]oxy]-2-hydroxybenzoic acid methyl ester, 0.6 ml (5 mmol) of benzyl bromide and 2.5 g (16.5 mmol) of potassium carbonate in 50 ml of acetone and 5 ml of DMF was stirred at reflux for 24 hours. After the usual workup, the crude product was recrystallized from ethyl acetate-hexane to give 1.5 g (89% yield, mp 85°-87°) of 5-[[6-([1,1'-biphenyl]-4-yloxy)hexyl]oxy]-2-(phenylmethoxy)benzoic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298652 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-818d8a2844b34520ae6da3a62e890ef0 |
| Source note | uspto-grants-1994_03 |