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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359131Generated: November 2, 2026

Diethanolamine → Benzenemethanol, 2,4-dichloro-α-methyl-, (αR)-

https://huagongshe.com/reaction/2359131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethanolamineHCID 8113—
Reactant2',4'-DichloroacetophenoneHCID 16693—
ReactantChlorobis((1S,2R,3S,5S)-2,6,6-trimethylbicyclo(3.1.1)hept-3-yl)boraneHCID 9923113—
SolventTetrahydrofuranHCID 8028—
ProductBenzenemethanol, 2,4-dichloro-α-methyl-, (αR)-HCID 695077382.2%

Reaction Conditions

Temperature-25 °C

Reaction Steps

To a solution of 2′,4′-dichloroacetophenone (10.9 g, 77.0 mmol) in anhydrous THF (80 mL) at −78° C. under nitrogen was slowly added a solution of (+)-B-chlorodiisopinocampheylborane ((+)-Ipc2BCl, 27.2, 85.0 mmol) in THF (15 mL). After the addition is complete, the reaction mixture was slowly warmed to −25° C. and stirred at this temperature for 2 h. The reaction mixture was then quenched with diethanolamine (17.9 g, 170 mmol), and stirred for 10 min. During this time, a solid formed and it was filtered off. The filtrate was dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified flash chromatography (SiO2, 0-20% ethyl acetate in hexanes) to give (R)-1-(2,4-dichlorophenyl)ethanol (12.0 g, 63.3 mmol, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685959B2
Source datasetuspto-grants-2014_04
ORD IDord-61a611dd92cd48f8b911ab1b1fe69787
Source noteuspto-grants-2014_04