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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378939Generated: October 30, 2026

Sodium hydride → HCID 86751260, compound

https://huagongshe.com/reaction/1378939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 86751261HCID 86751261—
SolventDichloromethaneHCID 6344—
ProductHCID 86751260HCID 86751260—

Reaction Steps

0.6 g of 2-(1-hydroxy-2'-methoxy-5'-bromo-benzyl)pyrazine were dissolved in 15 ml of methylene chloride. At 0° C., 0.2 g of NaH were added, resulting in the evolution of a gas and formation of a precipitate. 0.4 ml of trimethylacetyl chloride were added in one portion. The reaction mixture was stirred at room temperature overnight. The solvent was then stripped from the reaction mixture, and the residue was extracted with ice water and methylene chloride. The methylene chloride layer was washed with water, dried (MgSO4), filtered and stripped of the solvent to yield 0.9 g of 3-(1-trimethylacetoxy-2'-methoxy-5'-bromobenzyl)-pyrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670453
Source datasetuspto-grants-1997_09
ORD IDord-8f25f3c2c7f544618ae2cc6f683edae8
Source noteuspto-grants-1997_09