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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80234Generated: October 27, 2026

Acetic Acid → 3-Bromo-4-(pyrrolidin-1-ylmethyl)pyridine

https://huagongshe.com/reaction/80234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPyrrolidineHCID 31268—
Reactant3-Bromopyridine-4-carboxaldehydeHCID 2762997—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-4-(pyrrolidin-1-ylmethyl)pyridineHCID 5963613698.2%

Reaction Steps

Acetic acid (0.1 mL) was added to a stirred solution of 3-bromo-pyridine-4-carbaldehyde (220 mg, 1.18 mmol) and pyrrolidine (0.11 mL, 1.34 mmol) in DCE (15 mL) under nitrogen atmosphere and stirred at room temperature for 2 hours. This was followed by addition of NaBH(OAc)3 (342 mg, 1.612 mmol) at 0° C. over a period of 10 minutes. The resulting reaction mass was stirred for 12 hours at room temperature. The reaction was monitored by TLC (30% ethyl acetate in hexane). The reaction mixture was washed with NaHCO3 solution and extracted using ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to afford 275 mg of the product (98.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045173E1
Source datasetuspto-grants-2014_09
ORD IDord-6931c758e9b64d3abd05092f2e3a5a5a
Source noteuspto-grants-2014_09