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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577805Generated: October 26, 2026

Iodine → [2-((2R,6S)-2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-phenyl]-methanol

https://huagongshe.com/reaction/577805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium borohydrideHCID 4311764—
Reactant2-((2R,6S)-2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-benzoic acidHCID 67357511—
SolventTetrahydrofuranHCID 8028—
Product[2-((2R,6S)-2,6-Dimethyl-morpholin-4-yl)-3,4-difluoro-phenyl]-methanolHCID 67376655—

Reaction Steps

To a stirred and ice-bath cooled solution of 2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzoic acid (Intermediate 1, 27.0 g, 99.6 mmol) in THF (250 mL) was added sodium borohydride (12.56 g, 358.6 mmol) in small portions, followed by iodine (32.5 g, 139.4 mmol) in THF (250 mL). The addition was carried out such that the temperature maintained below 10° C. The mixture brought to room temperature and refluxed for 12 hours. It was cooled and then quenched with methanol (250 mL). Solvents were evaporated and the residue treated with 2M NaOH (500 mL) for 2 hours. The aqueous layer extracted with ethyl acetate (3×150 mL), and the combined organic phases were washed with water and brine before being dried (Na2SO4) and concentrated to give the title compound as a gummy solid. MS (ES) MH+: 257.2 for C13H17F2NO2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040528B2
Source datasetuspto-grants-2015_05
ORD IDord-0444590fbc2d4cd68acf83834a4f96f9
Source noteuspto-grants-2015_05