HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277384Generated: October 30, 2026
Isobutylene oxide → 2-Methyl-1-((4-(4-nitrophenoxy)quinolin-7-yl)oxy)propan-2-ol
https://huagongshe.com/reaction/2277384
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutylene oxide | HCID 11208 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(4-Nitrophenoxy)quinolin-7-ol | HCID 136350299 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-1-((4-(4-nitrophenoxy)quinolin-7-yl)oxy)propan-2-ol | HCID 68194257 | 42.7% |
Reaction Steps
To a flask containing 4-(4-nitrophenoxy)quinolin-7-ol (14.45 g, 45.33 mmol) was added a solution of sodium hydroxide (3.63 g, 90.66 mmol) in water/95% EtOH (90 mL/10 mL) followed by isobutylene oxide (12.12 mL, 136 mmol, pre-cooled to 0° C.). After stirring at 45° C. for 10 minutes, more isobutylene oxide (12.12 mL, 136 mmol, pre-cooled to 0° C.) was added. The reaction was continued to stir for additional 12 hours. The mixture was cooled to room temperature and continued to stir for 4 hours, then cooled to 0° C. and stirred for additional 10 minutes. The resulted solid was filtered, and then dissolved in DCM (130 mL). The solution was filtered and concentrated in vacuo. The residue was washed with petroleum ether (30 mL), and dried in vacuo at 45° C. overnight to afford the title compound as a yellow solid (6.86 g, 42.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133162B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-70c6776d94694798a3aa9559fd275461 |
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| Source note | uspto-grants-2015_09 |
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