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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1183674Generated: November 1, 2026

1,3-Dibromopropane → Ethyl 1-(3-(cyclopropylmethoxy)-4-nitrophenyl)cyclobutanecarboxylate

https://huagongshe.com/reaction/1183674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)acetateHCID 57995474—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-(3-(cyclopropylmethoxy)-4-nitrophenyl)cyclobutanecarboxylateHCID 5799551049%

Reaction Conditions

Temperature25 °C

Reaction Steps

Ethyl 2-(3-(cyclopropylmethoxy)-4-nitrophenyl)acetate (5 g, 17.9 mmol) was dissolved in 50 mL anhydrous DMF, NaH (60% wt. in oil, 1.43 g, 35.9 mmol) was added at 0° C. The reaction mixture was stirred for 0.5 h at 25° C. and 1,3-dibromopropane (1.91 mL, 17.9 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), dried over MgSO4, filtered and concentrated under reduced pressure to give ethyl 1-(3-(cyclopropylmethoxy)-4-nitrophenyl)cyclobutanecarboxylate (2.8 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664249B2
Source datasetuspto-grants-2014_03
ORD IDord-88f6ef8f14414af59fc0c1f3b3eb5078
Source noteuspto-grants-2014_03