HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-{4-[6-(4-Nonylphenyl)benzothiazol-2-yl]phenoxy}hexan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Bromo-1-hexanol | HCID 77970 | — |
| Reactant | 2-(4-Hydroxyphenyl)-6-(4-nonylphenyl)benzothiazole | HCID 135761779 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-{4-[6-(4-Nonylphenyl)benzothiazol-2-yl]phenoxy}hexan-1-ol | HCID 21924527 | 62% |
Reaction Steps
A solution of sodium hydroxide (0.08 g, 0.0020 mol) in water (20 cm3) was added dropwise to a solution of 4-[6-(4-nonylphenyl)benzothiazol-2yl]phenol (0.42 g, 0.0010 mol) in methanol (50 cm3). The 6-bromohexanol (0.18 g, 0.001 mol) was then added dropwise, followed by the potassium iodide (0.02 g, 0.00125 mol) in one portion. The reaction mixture was heated under reflux overnight and the poured onto a mixture of water (100 cm3) and 10% hydrochloric acid (20 cm3). The resultant precipitate was filtered off and recrystallised from ethanol to yield 0.31 g (62%) of the pure compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07118787B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-209622e8617c4fd7a94c296cb565df7a |
| Source note | uspto-grants-2006_10 |