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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087405Generated: October 31, 2026

3-Hydroxyacetophenone → 1-(3-{[(1S)-3-chloro-1-phenylpropyl]oxy}phenyl)ethanone

https://huagongshe.com/reaction/2087405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxyacetophenoneHCID 8487—
ReactantTriphenylphosphineHCID 11776—
Reactant(1R)-3-chloro-1-phenylpropan-1-olHCID 642409—
ReactantDiethyl azodicarboxylateHCID 5462977—
Product1-(3-{[(1S)-3-chloro-1-phenylpropyl]oxy}phenyl)ethanoneHCID 6952365876%

Reaction Steps

(1R)-3-Chloro-1-phenyl-1-propanol (1.000 g, 5.86 mmol), 1-(3-hydroxyphenyl)ethanone (0.797 9, 5.86 mmol), triphenylphosphine (1.54 g, 5.86 mmol) and diethylazodicarboxylate (1.53 g, 8.79 mmol) were combined in a flask, which was immediately flushed with argon. THF (20 mL) was added and the mixture was stirred overnight under argon. THF was removed in vacuo, the crude product was dissolved in 50 mL of CH2Cl2/H2O (1:1) and the organic layer was separated and dried over MgSO4. After removing the solvent in vacuo, the residue was purified by flash chromatography using 10% ethyl acetate/hexane to yield the desired product (900 mg, 76.0%): 1H NMR (400 MHz, CDCl3) δ 7.49-7.46 (m, 2H), 7.40-7.26 (m, 6H), 7.07-7.04 (m, 1H), 5.46-5.43 (dd, 1H, J=4.4 Hz, 8.8 Hz), 3.84-3.78 (m, 1H), 3.64-3.59 (m, 1H), 2.52 (s, 3H), 2.51-2.46 (m, 1H), 2.29-2.22 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727264B1
Source datasetuspto-grants-2004_04
ORD IDord-6f6ec586555a4c639422f1ab9648a2d6
Source noteuspto-grants-2004_04