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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639117Generated: November 3, 2026

2-Nitrophenol → 2,2-Dimethyl-5-(3-nitrophenoxy)pentanoic acid, methyl ester

https://huagongshe.com/reaction/1639117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-bromo-2,2-dimethylpentanoateHCID 13050502—
SolventAcetonitrileHCID 6342—
Product2,2-Dimethyl-5-(3-nitrophenoxy)pentanoic acid, methyl esterHCID 13171619894%

Reaction Steps

A mixture of 27.8 g (200 mmol) of 2-nitrophenol, 44.6 g (200 mmol) of methyl-5-bromo-2,2-dimethylpentanoate (Journal of Medicinal Chemistry, Vol. 26, pp 1020-1027 (1983)) and 30.5 g (220 mmol) of anhydrous potassium carbonate in 300 ml of acetonitrile is stirred at reflux for 18 hours. The inorganic salts are removed, washed with acetonitrile and the filtrate is concentrated on a rotary evaporator. The residue is taken up in diethyl ether and the solution washed with 2N potassium hydroxide (3×50 ml), brine, dried (magnesium sulfate), and evaporated to afford 55.9 g of crude product. Distillation gives 52.9 g of 2,2-dimethyl-5-(3-nitrophenoxy)pentanoic acid, methyl ester, bp 160°-165° C. (0.5 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04882357
Source datasetuspto-grants-1989_11
ORD IDord-63caa96182ae41a3a76e7051a837d16e
Source noteuspto-grants-1989_11