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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385875Generated: October 30, 2026

Sodium hydride → HCID 59526096, compound

https://huagongshe.com/reaction/385875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTetrahydro-2H-thiopyran-4-olHCID 576296—
Reactant2-Bromo-6-(bromomethyl)pyridineHCID 12954796—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59526096HCID 59526096—

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (0.24 g, 5.98 mmol) was suspended in tetrahydrofuran (19.9 mL) and cooled to 0° C. Tetrahydro-2H-thiopyran-4-ol (0.24 g, 1.99 mmol) was added and the reaction was stirred for 30 minutes. 2-Bromo-6-(bromomethyl)pyridine (Example 190, Step 1) (0.5 g, 1.99 mmol) was added and the reaction was warmed to and maintained at ambient temperature overnight. The reaction was diluted with ethyl acetate, quenched slowly with water, the layers were separated, and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over magnesium sulfate, filtered and concentrated. The crude mixture was purified by silica gel chromatography to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-6e0e1f6c7c7b4455b0cf352d9dac9624
Source noteuspto-grants-2013_02