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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705213Generated: October 24, 2026

(1R,2R)-2-Aminocyclohexanol → 3-(3,5-Difluorophenyl)oxetane

https://huagongshe.com/en/reaction/705213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R,2R)-2-AminocyclohexanolHCID 735777—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant(3,5-Difluorophenyl)boronic acidHCID 2734338—
Reactant3-IodooxetaneHCID 13356686—
CatalystNickel(II) iodideHCID 26038—
SolventIsopropanolHCID 3776—
Product3-(3,5-Difluorophenyl)oxetaneHCID 7065534063%

Reaction Steps

3,5-difluorophenylboronic acid (2.0 equiv.), (1R,2R)-2-aminocyclohexanol (0.06 equiv.), NaHMDS (2.0 equiv.), and nickel(II) iodide (0.06 equiv.) were dissolved in 2-propanol (0.35 M). The mixture was degassed with N2, stirred at rt for 10 min and then a solution of 3-iodooxetane (1.0 equiv.) in 2-Propanol (0.70 M) was added. The mixture was sealed and heated at 80° C. in the microwave for 20 min. The mixture was filtered through celite, eluting with EtOH and concentrated. The crude residue was purified by ISCO SiO2 chromatography eluting with 0-100% EtOAc in Heptanes to afford 3-(3,5-difluorophenyl)oxetane in 63% yield. 1H NMR (400 MHz, <cdcl3>) δ 6.88-6.96 (m, 2H), 6.72 (tt, J=2.20, 8.95 Hz, 1H), 5.08 (dd, J=6.26, 8.22 Hz, 2H), 4.71 (t, J=6.26 Hz, 2H), 4.14-4.24 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173883B2
Source datasetuspto-grants-2015_11
ORD IDord-43df638c606d45588962237d0b98474b
Source noteuspto-grants-2015_11