Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069727Generated: October 30, 2026

Formaldehyde → 2-Bromo-5-[(1-methyl-3-azetidinyl)oxy]pyridine

https://huagongshe.com/reaction/2069727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-(Azetidin-3-yloxy)-2-bromo-pyridine trifluoro-acetic acid saltHCID 86645086—
SolventDichloromethaneHCID 6344—
Product2-Bromo-5-[(1-methyl-3-azetidinyl)oxy]pyridineHCID 59473770104.2%

Reaction Steps

In a solution of 5-(Azetidin-3-yloxy)-2-bromo-pyridine trifluoro-acetic acid salt (0.5 g, 1.46 mmol) in dichloromethane (20 mL), add formaldehyde aqueous solution (37%, 0.58 mL, 7.29 mmol). Then add Na(OAc)3BH (0.774 g, 3.65 mmo) carefully. The reaction was stirred at room temperature under argon for 45 min. The reaction was quenched with water (30 mL), and then extracted with dichloromethane (3×20 mL). The combined organic phase was washed thoroughly with brine and water. Evaporation of solvent afford 2-Bromo-5-(1-methyl-azetidin-3-yloxy)-pyridine (0.37 g, yield 98%), which was pure enough for next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299077B2
Source datasetuspto-grants-2012_10
ORD IDord-9cca5c8ee4d745c3841362a2ae59b7ac
Source noteuspto-grants-2012_10