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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445109Generated: October 29, 2026

Sodium hydride → HCID 57422597, compound

https://huagongshe.com/reaction/445109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Methyl-4-[(4-methylbenzenesulfonyl)oxy]butan-2-olHCID 14001295—
ReactantHCID 178429280HCID 178429280—
SolventDimethylformamideHCID 6228—
ProductHCID 57422597HCID 5742259763.1%

Reaction Steps

To a suspension of sodium hydride (to which about 40% of a mineral oil was added, 0.23 g) in N,N-dimethylformamide (10 mL), 5-bromo-2-hydroxy-4-methylpyridine (1.00 g) was added under ice-cooling and the resultant reaction mixture was stirred for 30 minutes. To the reaction mixture, 3-hydroxy-3-methylbutyl 4-methylbenzene sulfonate (1.51 g) was added and the resultant reaction mixture was stirred at 60° C. for 4 hours. To the reaction mixture, a aqueous solution of saturated ammonium chloride was added and the resultant reaction mixture was extracted with ethyl acetate. The organic phase was washed with saturated saline and was dried over anhydrous sodium sulfate. From the organic phase, the solvent was distilled off under reduced pressure and the resultant residue was purified by silica gel column chromatography (eluate; n-hexane:ethyl acetate=50:50 to 33:67) to obtain the subject compound (0.92 g) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476287B2
Source datasetuspto-grants-2013_07
ORD IDord-91a0ba1013584c779780840da3477c52
Source noteuspto-grants-2013_07