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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978499Generated: October 29, 2026

Sodium hydride → HCID 86756772, compound

https://huagongshe.com/reaction/1978499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 21994033HCID 21994033—
Reactant5-Thia-1,8b-diazaacenaphthylene-4-carbaldehydeHCID 21994144—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductHCID 86756772HCID 86756772—

Reaction Steps

To a solution of 2.01 g (4.87 mM) of tert-butyl 4-(diethoxyphosphorylmethanesulfonylmethyl)piperidine-1-carboxylate in 30 ml of toluene was added 0.18 g (4.43 mM) of a 60% suspension of sodium hydride in liquid paraffin at room temperature, and the mixture was stirred at the prevailing temperature for 1 hour. This reaction mixture was added to a solution of the above crude 5-thia-1,8b-diazaacenaphthylene-4-carbaldehyde in N,N-dimethylformamide (10 ml)-toluene (30 ml) at room temperature and the mixture was stirred at the prevailing temperature for 0.5 hour. This reaction mixture was poured in water and extracted with 3 portions of ethyl acetate. The organic layers were pooled and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate˜ethyl acetate/methanol=9/1) to provide crude (E)-4-[2-[1-(tert-butoxycarbonyl)piperidin-4-ylmethane-sulfonyl]viny]-5-thia-1,8b-diazaacenaphthylene. This crude product was not purified but used as it was in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235731B1
Source datasetuspto-grants-2001_05
ORD IDord-45c52aeeaa3f4fafad9b5754c852ed8d
Source noteuspto-grants-2001_05