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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537384Generated: October 29, 2026

1-Chloro-2-[(1E)-prop-1-en-1-yl]benzene → HCID 66634192, compound

https://huagongshe.com/reaction/537384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-[(1E)-prop-1-en-1-yl]benzeneHCID 14419677—
Reactant1-((1R)-((2R,4R,5S)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)-4-((1R)-((2R,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)phthalazineHCID 51003674—
Reactant2-Methylpropan-2-ol--water (1/1)HCID 71401949—
ProductHCID 66634192HCID 6663419290%

Reaction Steps

1-(2-chlorophenyl)-trans-1-propene (1.5 g, Preparation Example 1) was dissolved in 30 mL of the mixture of t-BuOH/H2O (1:1 (V/V)). At 0° C., AD-mix-α (Aldrich, U.S.A.) (13.7 g) and methane sulfone amide (CH3SO2NH2, 0.76 g, 0.0080 mol) were added thereto and stirred for overnight. When the reaction was completed, the obtained product was washed with an aqueous solution of sodium sulfite (Na2SO3) and ethylacetate (EA). Then, the organic layer was dehydrated with anhydrous magnesium sulfate (MgSO4), filtrated, and concentrated under reduced pressure. The concentrated residue was purified by a silica gel column chromatography to produce the title compound (1.65 g, yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859817B2
Source datasetuspto-grants-2014_10
ORD IDord-7dca4f013be74266bb0af7feffd2a31a
Source noteuspto-grants-2014_10