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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335487Generated: October 28, 2026

Potassium Hydroxide → 3-(1-Methylpyrrolidin-2-yl)pyridine

https://huagongshe.com/reaction/335487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant(R,S)-1-METHYL-3-NICOTINOYLPYRROLIDONEHCID 4069086—
ReactantPotassium borohydrideHCID 4192641—
SolventHydrochloric AcidHCID 313—
Product3-(1-Methylpyrrolidin-2-yl)pyridineHCID 94267.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-methyl-3-nicotinoyl-2-pyrrolidone (20.4 g, 0.1 mol) was dissolved in a 6N hydrochloric acid (150 mL) The solution was heated to 100° C. to react for 24 h and then cooled to room temperature. The pH of the solution was adjusted to 7 by using KOH under an ice bath, and then potassium borohydride (5.3 g, 0.1 mol) was added therein and the temperature was back to room temperature for 2 h. 200 mL Distilled water was added and the mixture was then stream-distilled. The distilled water phase was extracted with 300 mL petroleum ether, and the resultant petroleum ether was concentrated till dry to give a colorless oily product (11.0 g). HPLC purity 99.2%; 1H NMR (CDCl3, 300 MHz) δ: 8.52 (d, 1H), 8.48 (dd, 1H), 7.69 (dt, 1H), 7.25 (dd, 1H), 3.23 (t, 1H), 3.07 (t, 1H), 2.29 (m, 1H), 2.16 (s, 3H), 1.90-2.04 (m, 2H), 1.65-1.88 (m, 2H), ESI-MS 163.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08884021B2
Source datasetuspto-grants-2014_11
ORD IDord-9dabe0261d564e4abef716f34b6c5d8f
Source noteuspto-grants-2014_11