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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609402Generated: October 26, 2026

Hydrogen iodide → Orcinol

https://huagongshe.com/reaction/1609402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen iodideHCID 24841—
Reactant3,5-DimethoxytolueneHCID 77844—
ProductOrcinolHCID 10436—

Reaction Steps

Methylmagnesium bromide (35 g) was added to 1,3-dimethoxy-5-benzoyl chloride (100 g) to obtain 1,3-dimethoxy-methylphenone in a yield of 45%. Then, the reduction was conducted by adding water (300 cc), concentrated hydrochloric acid (300 cc) and 1,3-dimethoxy-methylphenone (100 g) to zinc amalgam obtained from zinc (400 g) and mercuric chloride (20 g). Further, concentrated hydrochloric acid (10 to 15 cc) was added every one hour. After the completion of the reaction, the reaction solution was cooled and saturated with sodium chloride, and then extracted with ether to obtain 40 g of 1,3-dimethoxy-5-methylbenzene. Hydrogen iodide was added to the resulting 1,3-dimethoxy-5-methylbenzene and stirred at 115° to 125° C. for 3 hours under nitrogen atmosphere. After cooling, the product was extracted with methylene chloride to obtain 30 g of 5-methylresorcinol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399785
Source datasetuspto-grants-1995_03
ORD IDord-95315044872d4612af294f918464c28a
Source noteuspto-grants-1995_03