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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20055Generated: October 26, 2026

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

https://huagongshe.com/reaction/20055

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 9h 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 numberUS07745484B2
Source datasetuspto-grants-2010_06
ORD IDord-9e879ac3aa344099b227c59bf71a01e4
Source noteuspto-grants-2010_06