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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73641Generated: October 28, 2026

4-Fluoroaniline → HCID 66582141, compound

https://huagongshe.com/reaction/73641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroanilineHCID 9731—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 86668662HCID 86668662—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66582141HCID 66582141—

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolved 55 uL 4-fluoroaniline in 1.3 mL CH2Cl2 then cooled to 0° C. and added 0.21 mL AlMe3 (2.0M in toluene). Warmed to RT, stirred for 30 minutes, then added 50 mg (1aS,4aR,8aS)-hexahydro-1aH,6H-oxireno[e]chromene (7-5) in 1.0 mL CH2Cl2. Stirred for two hours at RT, then sat. sodium potassium tartrate solution was added dropwise to the reaction, allowing gas evolution to cease between drops, until no further gas evolution was noted. The mixture was diluted with water, then extracted with CH2Cl2. The extract was dried over Na2SO4, filtered, concentrated, then purified on silica (0-40% EtOAc in hexanes) to yield the title compound. 1H NMR (500 MHz, CDCl3) δ=1.42-1.69 (m, 7H), 1.90-2.09 (m, 3H), 2.47 (s, 1H), 3.38-3.48 (m, 3H), 3.53 (s, broad, 1H), 3.92-3.95 (m, 1H), 6.54-6.59 (m, 2H), 6.84-7.26 (m, 2H) ppm. HRMS (ES) m/z M±H calc'd: 266.1551. found 266.1551.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829196B2
Source datasetuspto-grants-2014_09
ORD IDord-56369c6cbce64a48b452e9793acf978a
Source noteuspto-grants-2014_09