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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464384Generated: October 29, 2026

Benzyl Chloride → HCID 20212031, compound

https://huagongshe.com/reaction/464384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
ReactantHCID 20212017HCID 20212017—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 20212031HCID 2021203194%

Reaction Steps

2-Iodo-3-hydroxy-5-methylpyridine (13.5 g, 57.4 m.mole) was added to a solution of sodium ethoxide (57.4 m.mole, prepared freshly from sodium and dry ethanol (100 ml). Dry dimethyl sulfoxide (250 ml) was added, and the ethanol was removed by distillation under reduced pressure. Benzyl chloride (7.27 g, 57.4 mole) was added portionwise with cooling and then the mixture was heated at 90°-100° for 15 hours. The dimethyl sulfoxide was boiled off under reduced pressure, water was added (100 ml) and the product was extracted from this with chloroform. After drying with magnesium sulfate and evaporation under reduced pressure, a crude product was obtained (17.62 g, 94% yield) a tiny portion of which, after heating in water and the recrystallising from methanol-water, gave 2-iodo-3-benzyloxy-5-methylpyridine which was pure by N.M.R. (mp 83°-5°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547512
Source datasetuspto-grants-1985_10
ORD IDord-f3a6212a7344453a946903d14fe98a6d
Source noteuspto-grants-1985_10