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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385468Generated: October 31, 2026

1-Bromo-2-methylpropane → Ethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)-4-methylpentanoate

https://huagongshe.com/reaction/385468

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-methylpropaneHCID 6555—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)acetateHCID 57995474—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)-4-methylpentanoateHCID 5799550878.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

Ethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)acetate (2.2 g, 7.8 mmol) was dissolved in 20 mL anhydrous DMF and NaH (60% wt. in oil, 0.189 g, 7.8 mmol) was added at 0° C. The reaction mixture was stirred for 0.5 h at 25° C. and isobutyl bromide (1.08 g, 7.8 mmol) was added drop wise at 0° C. The reaction mixture was stirred at 0° C. for 1 h and saturated NH4Cl solution (10 mL) was added. The reaction mixture was extracted with EtOAc (3×20 mL) and the combined organic phases were washed with water (3×20 mL) and brine (20 mL), and dried over MgSO4, filtered and concentrated under reduced pressure to give ethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)-4-methylpentanoate (2.06 g) of colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367863B2
Source datasetuspto-grants-2013_02
ORD IDord-94153fc05b8a44e0a6f30789580b8809
Source noteuspto-grants-2013_02