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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576469Generated: October 30, 2026

4-Methyl-2-Pentanol → (alphaS)-alpha-Methyl-3,5-bis(trifluoromethyl)benzenemethanol

https://huagongshe.com/reaction/576469

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-2-PentanolHCID 7910—
Reactant1-(3,5-Bis(trifluoromethyl)phenyl)ethan-1-oneHCID 121616—
ReactantNadhHCID 439153—
CatalystZincchlorideHCID 3007855—
SolventGlycerolHCID 753—
Product(alphaS)-alpha-Methyl-3,5-bis(trifluoromethyl)benzenemethanolHCID 9816575—

Reaction Steps

For the conversion, a mixture of 1 mL of a buffer (100 mM TEA, pH=7, 10% glycerol, 1 mM ZnCl2), 3 ml 4-methyl-2-pentanol, 1 ml 1-[3,5 bis-(trifluoro-methyl)phenyl]ethane-1-one, 2 mg NAD and 0.7 kU recombinant oxidoreductase from Microbacterium spec. DSMZ 20028 was incubated at room temperature for 24 h with constant thorough mixing. After 24 h, more than 90% of the 1-[3,5 bis-(trifluoro-methyl)phenyl]ethane-1-one used had been reduced to (1S)-1[3,5-bis(trifluoromethyephenyl)ethane-1-ol. Subsequently, the 4-methyl2-pentanol phase containing the product was separated from the aqueous phase, filtered, and the product (1S)-1[3,5-bis(trifluoromethyl)phenyl]ethane-1-ol was obtained by distillation. The crude product (1S)-1-[3,5-bis(trifluoromethyl)phenyl]ethane-1-one obtained in this manner exhibited an enantiomeric excess of >99.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040265B2
Source datasetuspto-grants-2015_05
ORD IDord-594b41e889de4c7aa6dbcbfc849d5148
Source noteuspto-grants-2015_05