Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022845Generated: October 30, 2026

Pentanal → HCID 67447069, compound

https://huagongshe.com/reaction/1022845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentanalHCID 8063—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesium BromideHCID 82241—
Reactant3-(4-Bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazoleHCID 23159812—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventPentaneHCID 8003—
ProductHCID 67447069HCID 6744706945%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-(4-bromo-3-methyl-phenyl)-5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazole (500 mg) in ether (20 mL) was added tert-butyllithium (1.5 mL of a 1.6 M solution in pentane) at −78° C. After 10 min at this temperature, MgBr2 (0.15 M in THF, 10.3 mL) was added dropwise and left for another 15 min. Valeraldehyde (141 μL, 114 mg) was added and the mixture was stirred at −78° C. for 1 h before it was allowed to warm to room temperature over night. Saturated aqueous NH4Cl solution was added and the mixture was extracted with MTBE. The organic layer was separated, dried (Na2SO4) and concentrated in vacuum. The residue was purified by flash chromatography on silica gel to yield the title compound (230 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722673B2
Source datasetuspto-grants-2014_05
ORD IDord-af57652bd6b745969d35c35f61c930da
Source noteuspto-grants-2014_05