HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73639Generated: October 28, 2026
4-Fluoroaniline → (4aR,5R,8aS)-5-[(4-fluorophenyl)amino]octahydro-4-aH-isochromen-4a-ol
https://huagongshe.com/reaction/73639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 86668661 | HCID 86668661 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4aR,5R,8aS)-5-[(4-fluorophenyl)amino]octahydro-4-aH-isochromen-4a-ol | HCID 52912157 | — |
Reaction Steps
To a mixture of 4-fluoroaniline (0.119 g, 1.07 mmol) in CH2Cl2 (1 mL) at 0° C. was added trimethylaluminum (2M in toluene, 0.535 mL) dropwise. The mixture was warmed to rt and stirred for 30 min. A mixture of cis and trans octahydrooxireno[e]isochromene (0.033 g, 0.214 mmol) in CH2Cl2 (1 mL) was then added and the mixture was stirred at rt overnight. The reaction mixture was cooled to 0° C. and treated with 50% NaOH (1 mL) then water (1 mL). It was diluted with more water and extracted 3× with CH2Cl2. The combined organics were dried, filtered and concentrated. The residue was purified by column chromatography to give the title compound. 1H NMR (500 MHz, CDCl3) δ 6.92 (t, 2H, J=8.8 Hz), 6.71 (dd, 2H, J=4.2 Hz, 8.8 Hz), 3.81-3.87 (m, 1H), 3.61 (dd, 1H, J=4.6 Hz, 11.2 Hz), 3.50 (t, 1H, J=11.0 Hz), 3.32 (s, 1H), 2.15-2.26 (m, 1H), 1.89-2.07 (m, 2H), 1.59-1.69 (m, 2H), 1.45-1.58 (m, 1H), 1.20-1.37 (m, 4H). HRMS (ES) m/z M+H calc'd.: 266.1551. found: 266.1549
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08829196B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-f267c5b6862a4c7d8241a8196ef2163a |
|---|
| Source note | uspto-grants-2014_09 |
|---|