HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26360Generated: October 29, 2026
Salicylaldehyde → HCID 21322966, compound
https://huagongshe.com/reaction/26360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21322965 | HCID 21322965 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21322966 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04150034 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-aef4b367bf7948c0b26b53cd938af759 |
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| Source note | uspto-grants-1979_04 |
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