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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26360Generated: October 29, 2026

Salicylaldehyde → HCID 21322966, compound

https://huagongshe.com/reaction/26360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantTriethylamineHCID 8471—
ReactantHCID 21322965HCID 21322965—
SolventTolueneHCID 1140—
ProductHCID 21322966HCID 21322966—

Reaction Steps

3.1 g (0.0254 moles) of salicylic aldehyde are dissolved in 30 ml of anhydrous toluene and 8.1 g (0.025 moles) of N-methyl-carbamic acid-pentachlorophenyl-ester are added under stirring at room temperature, whereafter 2.6 g (0.0257 moles) of triethylamine are added to the mixture under stirring. During the addition of the triethylamine an elevation of the temperature of about 2°-5° C. may be observed. The reaction mixture is stirred at 25°-30° C. for 2 hours, after about 1 hour the reaction mixture becomes clear. The unreacted active ester is filtered, the toluene is removed from the filtrate and the residual oily substance is recrystallized from a three-fold amount of diisopropylether. 2-methyl-carbamoyloxy-benzaldehyde is obtained. Mp.: 128°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150034
Source datasetuspto-grants-1979_04
ORD IDord-aef4b367bf7948c0b26b53cd938af759
Source noteuspto-grants-1979_04