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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485178Generated: October 29, 2026

Sodium Iodide → HCID 20271551, compound

https://huagongshe.com/reaction/485178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 5-bromovalerateHCID 84580—
Reactant6-Hydroxy-2,3-dimethoxybenzaldehydeHCID 13092115—
SolventEthanolHCID 702—
ProductHCID 20271551HCID 20271551—

Reaction Steps

2,3-Dimethoxy-6-hydroxybenzaldehyde (5.46 g, 0.03 M), ethyl 5-bromopentanoate (6.273 g, 0.03 M), anhydrous potassium carbonate (4.45 g), sodium iodide (0.185 g) and 95% ethanol (25 ml) were reacted together in an analogous manner to that described in example 2(F) to give ethyl 5-(2-formyl-3,4-dimethoxyphenoxy)pentanoate as an oil. This ester was demethylated with magnesium iodide (from 7.18 g iodine) in an analogous manner to that described in example 2(C), except that the ethyl acetate solution obtained on work-up of the demethylation was extracted with 2 N sodium hydroxide solution. The combined extracts were acidified with conc. hydrochloric acid and the oily product extracted into ether. The combined extracts were washed with water, extracted with sodium bicarbonate solution and the combined extracts acidified to give a solid which was filtered off, washed with water and dried. The product was passed through a column of kieselgel eluting with chloroform-methanol (95:5) and the purified product was recrystallsedfrom benzene, m.p. 105°-107° C. (Found: C, 58.43; H, 3.96. C13H16O2 requires C, 58.20; H, 6.01%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535183
Source datasetuspto-grants-1985_08
ORD IDord-578d56355572407499d56e742a2a169e
Source noteuspto-grants-1985_08