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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712646Generated: October 25, 2026

Sodium hydride → 3-Bromo-5-(3-methanesulfonyl-propoxymethyl)-pyridine

https://huagongshe.com/reaction/712646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(Methylsulfonyl)-1-propanolHCID 200424—
Reactant3-Bromo-5-(bromomethyl)pyridineHCID 14932948—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-5-(3-methanesulfonyl-propoxymethyl)-pyridineHCID 11766742299%

Reaction Steps

3-Methanesulfonyl-propan-1-ol (69 mg, 0.50 mmol) is dissolved in 2.0 mL of DMF and 60% sodium hydride (20 mg, 0.50 mmol) is added at 0° C. The mixture is stirred for 15 min and 3-bromo-5-bromomethyl-pyridine (50 mg, 0.20 mmol) is added. The mixture is stirred for 2 hrs and saturated aqueous NH4Cl solution (3 mL) is added along with water (10 mL) and EtOAc (10 mL). The mixture is stirred for 10 min and the aqueous layer is separated and extracted with EtOAc (2×15 ml). The organic layers are combined and concentrated to give the crude product. Purification by flash column chromatography affords 61 mg of 3-bromo-5-(3-methanesulfonyl-propoxymethyl)-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-ad44a76cf9a24adb888cb67d40b49d5f
Source noteuspto-grants-2015_11