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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515911Generated: October 31, 2026

Sodium hydride → HCID 69431554, compound

https://huagongshe.com/reaction/515911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-MorpholinoethanolHCID 61163—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69431554HCID 69431554—

Reaction Conditions

Temperature0 °C

Reaction Steps

NaH (1.0 g, 25.0 mmol, 60% in oil) suspended in anhydrous tetrahydrofuran is cooled at 0° C. in an ice bath under argon, and then 2-morpholinoethanol (2.7 g, 20.7 mmol) is added dropwise. The ice bath is withdrawn and the suspension is stirred for 1 hour at ambient temperature. 5-Bromo-2-chloro-pyrimidine (4.0 g, 20.7 mmol) is then added at ambient temperature and the reaction mixture is stirred for 16 hours at ambient temperature. Saturated aqueous ammonium chloride solution (10 mL) and water (10 mL) are added to the reaction mixture; the pH is adjusted to 9 by adding saturated aqueous NaHCO3 solution. The resulting solution is extracted 3 times with ethyl acetate, the organic phase is then washed with brine, dried over MgSO4, and then evaporated to dryness. The expected compound precipitates out by means of the addition of petroleum ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-b6f751933534466e9fc9a3b057c65513
Source noteuspto-grants-2015_08