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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336231Generated: October 29, 2026

Water → 3-nitro-4-pyrrolidin-1-ylbenzoic acid

https://huagongshe.com/reaction/336231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantPyrrolidineHCID 31268—
ReactantEthyl 4-fluoro-3-nitrobenzoateHCID 21277355—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-nitro-4-pyrrolidin-1-ylbenzoic acidHCID 367193090%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 4-fluoro-3-nitrobenzoate (Chontech 01072; 500 mg; 2.35 mmol; 1 eq.) and pyrrolidine (Fluka 83240; 500.48 mg; 7.04 mmol; 3 eq.) in DMF (2 mL) was stirred at 60° C. for 4 hours. The reaction mixture was then partitioned between ethyl acetate and aq. NH4Cl. The organic layer was washed three times with aq. NH4Cl then brine, dried over magnesium sulfate and concentrated in vacuo to give a yellow oil. The latter was taken up in THF (5 mL) and lithium hydroxide (280.86 mg; 11.73 mmol; 5 eq.) then water (5 mL) were added. The reaction mixture was stirred at room temperature for 16 hours then the THF was evaporated and the residue was diluted with water. After acidification with AcOH, the formed precipitate was filtered and dried under high vacuum to afford the title compound (497 mg, 90%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889668B2
Source datasetuspto-grants-2014_11
ORD IDord-6e23f178f2c341a1bbfaf8a42dafbc49
Source noteuspto-grants-2014_11