Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73632Generated: October 29, 2026

4-Fluoroaniline → HCID 68154261, compound

https://huagongshe.com/reaction/73632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroanilineHCID 9731—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 86668658HCID 86668658—
SolventDichloromethaneHCID 6344—
ProductHCID 68154261HCID 68154261—

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 and stirred to rt for 30 min. (1aS,5aS)-hexahydro-4H-oxireno[i]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 6.84-6.90 (m, 2H), 6.51-6.57 (m, 2H), 3.90-3.97 (m, 1H), 3.50-3.64 (m, 3H), 3.35-3.45 (m, 2H), 2.61 (s, 1H), 1.95-2.04 (m, 1H), 1.32-1.75 (m, 8H). HRMS (ES) m/z M+H cal'd: 266.1551. found: 266.1548.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829196B2
Source datasetuspto-grants-2014_09
ORD IDord-92409a60ae7d47e085907fc1f6291ae9
Source noteuspto-grants-2014_09