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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009163Generated: October 25, 2026

Hydrochloric Acid → (4R)-6-bromo-2-methyl-2-(trifluoromethyl)chroman-4-ol

https://huagongshe.com/reaction/1009163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant(3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaboroleHCID 2734713—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant6-Bromo-2-methyl-2-(trifluoromethyl)chroman-4-oneHCID 67305602—
SolventTolueneHCID 1140—
Product(4R)-6-bromo-2-methyl-2-(trifluoromethyl)chroman-4-olHCID 67305384—

Reaction Steps

To a cooled (ice bath) solution of (s)-2-methyl-cbs-oxazaborolidine 1.0 M in toluene (100 μl, 100 μmol) was added borane-dimethyl sulfide 2.0 M in THF (500 μl, 1000 μmol). After stirred 15 min, a solution of 6-bromo-2-methyl-2-(trifluoromethyl)chroman-4-one (309 mg, 1000 μmol) in toluene was added drop wise. The reaction was completed after stirring 9 h at 0° C. 2N HCl was added slowly to quench the reaction. The resulted mixture was extracted with EtOAc. The organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated. The residue was purified on silica gel column to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973047B2
Source datasetuspto-grants-2011_07
ORD IDord-2396bf1544d14e289ddb24fecf91e9d5
Source noteuspto-grants-2011_07