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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516203Generated: October 30, 2026

HCID 90200234, compound → HCID 90200042, compound

https://huagongshe.com/reaction/516203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 90200234HCID 90200234—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 90200042HCID 9020004290%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(3-Chlorophenyl)-3-iodopropan-1-one: Intermediate 12A (2.415 g, 8.14 mmol) was dissolved in acetone (40.7 mL) and the above solution was cooled to 0° C. and Jones Reagent (6.08 ml, 16.29 mmol) was added dropwise. The reaction mixture turned orange/brown and was allowed to stir at 0° C. for 30 min. To the mixture was added 10 mL of isoproponal (reaction mixture turned green) and was then allowed to stir at rt for 10 min. The reaction mixture was then diluted with EtOAc and water. The organic layer was washed with water (3×) and brine, dried with magnesium sulfate, filtered and concentrated to yield a light yellow oil (which solidified into long yellow needles). The crude product was then purified using silica gel chromatography to yield the desired product as a white solid (2.16 g, 90%). MS (ESI) m/z: 294.8 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 7.93 (t, J=1.6 Hz, 1H), 7.85-7.81 (m, 1H), 7.59-7.56 (m, 1H), 7.47-7.42 (m, 1H), 3.65-3.60 (m, 2H), 3.49-3.43 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108981B2
Source datasetuspto-grants-2015_08
ORD IDord-f03c5595818648f3b13bc2fe0dbc0dd0
Source noteuspto-grants-2015_08