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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357619Generated: October 30, 2026

Sodium hydride → Ammonia

https://huagongshe.com/reaction/357619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
ReactantHCID 178513139HCID 178513139—
SolventDimethylformamideHCID 6228—
ProductAmmoniaHCID 222—
ProductHCID 178495984HCID 178495984—

Reaction Steps

2.88 g (0.06 mol) of sodium hydride dispersion (approximately 50% in oil; Fluka, Buchs, Switzerland) are added in portions over a period of 10 minutes, with stirring and with the introduction of nitrogen, to a solution of 8.1 g (0.05 mol) of benzaldehyde guanylhydrazone in 80 ml of DMF. After 25 minutes stirring at room temperature, 7.1 ml (0.06 mol) of bromoacetaldehyde dimethylacetal (Aldrich, Buchs, Switzerland; 97%, Cat. no. 24,250-0) are added dropwise to the mixture, which has been cooled in an ice-bath. The reaction mixture is stirred for one hour at room temperature and for 20 hours at 55° C., and then concentration by evaporation is carried out in vacuo and the residue is partitioned between ethyl acetate and water. The organic phase is washed with water and brine and is concentrated by evaporation, and the oily residue is purified by flash chromatography on silica gel having a particle size of 0.04-0.063 mm, using ethyl acetate and ethyl acetate/methanol (9:1). Concentration of the product-containing fractions by evaporation yields the title compound in the form of an oil, Rf value=0.80 (silica gel/methylene chloride:methanol:conc. ammonia (40:10:1)), 1H-NMR (DMSO): δ=8.07 (s, 1H); 7.67-7.73 (m, 2H); 7.23-7.40 (m, 3H); 5.93 (bs, 3H); 4.48 (t, 1H); 3.32 (s, 6H); 3.29 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840911
Source datasetuspto-grants-1998_11
ORD IDord-c38ccc24f55f47ee8e1e9dd9e861efcb
Source noteuspto-grants-1998_11