HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73627Generated: October 29, 2026
4-Fluoroaniline → (4R,4aR,8aR)-4-[(4-fluorophenyl)amino]octahydro-4-aH-isochromen-4a-ol
https://huagongshe.com/reaction/73627
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 86668657 | HCID 86668657 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4R,4aR,8aR)-4-[(4-fluorophenyl)amino]octahydro-4-aH-isochromen-4a-ol | HCID 52911327 | — |
Reaction Steps
To a mixture of 4-fluoroaniline (0.721 g, 6.48 mmol) in CH2Cl2 (6 mL) at 0° C. was added trimethylaluminum (2M in toluene, 3.24 mL) dropwise. The mixture was warmed to rt for 30 min. A mixture of both cis and trans octahydrooxireno[d]isochromene (0.200 g, 1.30 mmol) in CH2Cl2 2 mL+0.5 mL rinse) was then added and the mixture was stirred at rt overnight. The reaction was cooled to 0° C. and treated with 50% NaOH (1 mL) then water (1 mL). The mixture was diluted with more water and extracted 3× with CH2Cl2. The combined organics were dried (anhd. Na2SO4), filtered, and concentrated. The residue was purified by column chromatography to give the title compound. 1H NMR (500 MHz, CDCl3) δ 6.94 (1, 2H, J=8.6 Hz), 6.78 (dd, 2H, J=4.2 Hz, 8.8 Hz), 4.14 (dd, 1H, J=1.5 Hz, 12.0 Hz), 3.64 (d, 1H, J=11.5 Hz), 3.56 (dd, 1H, J=4.6 Hz, 11.0), 3.48 (t, 1H, J=11.5 Hz), 3.10 (s, 1H), 1.17-2.00 (m, 9H). HRMS (ES) m/z M+H calc'd.: 266.1551. found: 266.1554
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829196B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2c1f9f1629524a2fae648bea43e04d09 |
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| Source note | uspto-grants-2014_09 |
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