Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253804Generated: October 30, 2026

Sodium hydride → HCID 57422597, compound

https://huagongshe.com/reaction/1253804

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 saturated ammonium chloride aqueous solution was added and the resultant reaction mixture was extracted with ethyl acetate. The organic phase was washed with a 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 pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455500B2
Source datasetuspto-grants-2013_06
ORD IDord-8451baa5a8b6460b9e8b201a592f0741
Source noteuspto-grants-2013_06