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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465125Generated: November 3, 2026

Methyl iodide → HCID 59394935, compound

https://huagongshe.com/reaction/1465125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCesium carbonateHCID 10796—
ReactantHCID 59395034HCID 59395034—
SolventDimethylformamideHCID 6228—
ProductHCID 59394935HCID 5939493589%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-bromo-2-cyclopentyl-5-nitro-phenol (310 mg, 1.08 mmol) and Cs2CO3 (529 mg, 1.62 mmol) in DMF (2.0 mL) was added iodomethane (769 mg, 337 μL, 5.42 mmol) dropwise. The reaction was stirred at 50° C. under inert atmosphere for 16 h. The reaction was quenched with water and the aqueous layer was extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated. Purification by silica gel chromatography (0-20% ethyl acetate/hexane) provided 1-bromo-5-cyclopentyl-4-methoxy-2-nitrobenzene as a light yellow oil (288 mg, 89% yield). 1H NMR (400.0 MHz, DMSO-d6) 7.65 (d, J=6.6 Hz, 2H), 3.87 (s, 3H), 3.29-3.21 (m, 1H), 1.99-1.91 (m, 3H), 1.81-1.50 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999976B2
Source datasetuspto-grants-2015_04
ORD IDord-ca28747268c5465d83b9edfd9a5668ec
Source noteuspto-grants-2015_04