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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272931Generated: October 25, 2026

Potassium Iodide → HCID 59837421, compound

https://huagongshe.com/reaction/272931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantCesium carbonateHCID 10796—
Reactant(2R)-2-(Methoxymethyl)pyrrolidineHCID 671216—
ReactantHCID 23091704HCID 23091704—
Reactant1-[4-(3-Bromo-propoxy)-phenyl]-cyclohexanecarbonitrileHCID 59837504—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductAmmoniaHCID 222—
ProductHCID 59837421HCID 5983742154%

Reaction Conditions

Temperature75 °C

Reaction Steps

A (1:3) mixture of 1-[4-(3-bromo-propoxy)-phenyl]-cyclohexanecarbonitrile and 1-[4-(3-chloro-propoxy)-phenyl]-cyclohexanecarbonitrile (2.00 g, 7.20 mmol), Cs2CO3 (2.58 g, 7.20 mmol), potassium iodide (0.20 g, 1.20 mmol) and (R)-(−)-2-(methoxymethyl)pyrrolidine (1.07 mL, 8.60 mmol) in NMP (20 mL) was heated to 75° C. overnight. The reaction mixture was cooled to ambient temperature, concentrated in vacuo, and quenched by adding water (30 mL). The crude product was extracted with ethyl acetate (30×mL) and the organic extracts were dried over Na2SO4, filtered and concentrated in vacuo. The compound was purified by column chromatography on Biotage® silica gel, eluting with dichloromethane:methanol:ammonia, 100:0:0 to 90:10:1 to give the title compound as a brown oil (1.39 g, 54%). 1H NMR (400 MHz, CDCl3) δ 7.38 (d, 2H), 6.70 (d, 2H), 4.02 (t, 2H), 3.46-3.38 (m, 1H), 3.36-3.28 (m, 3H), 3.24-3.16 (m, 1H), 3.12-3.04 (m, 1H), 2.72-2.58 (m, 1H), 2.52-2.44 (m, 1H), 2.30-2.20 (m, 1H), 2.18-2.06 (m, 2H), 1.98 (pentet, 2H), 1.92-1.60 (m, 12H), 1.36-1.18 (m, 1H); HRMS (ESI+) 357.2537 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456164B2
Source datasetuspto-grants-2008_11
ORD IDord-439af9c4efb94e9586d82a556bc5af98
Source noteuspto-grants-2008_11