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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194388Generated: October 31, 2026

Methane → HCID 178519558, compound

https://huagongshe.com/reaction/1194388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178431335HCID 178431335—
SolventWaterHCID 962—
ProductHCID 178519558HCID 178519558804.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

82.83 g (0.0339 mole) of 4-[(2,2-dimethyl-4H-1,3-benzodioxin-8-yl)methyl]-1H-imidazole (prepared in Example 5.2.) are suspended in 1645 ml of water (pH 7.9) and dissolved by the addition, over the course of 80 minutes, of 349 ml of a 1N aqueous solution of hydrochloric acid. When this addition is complete, the pH of the solution is 2.5. The reaction mixture is subsequently heated for 1 hour on an oil bath at 120° C. The solution is then cooled, treated with 5 g of Norit and filtered on Hyflo-cel. The solution is subsequently rendered alkaline by the addition of 242.5 ml of a 1N aqueous solution of sodium hydroxide (pH 8.5). The precipitate obtained is filtered off, washed with water and dried. This precipitate is then dissolved in 3.3 liters of ethyl acetate in the presence of Norit and of a few grams of sodium sulfate. The mixture is then filtered, concentrated to a volume of 400 ml and left to crystrallize. There are obtained 55.67 g of 3-[(1H-imidazol-4-yl)methyl]-2-hydroxybenzenemethanol. Yield: 80.4% of theory; M.P.: 152°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814343
Source datasetuspto-grants-1989_03
ORD IDord-14592daf941f40ba95bbd937410caa97
Source noteuspto-grants-1989_03