HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249690Generated: October 29, 2026
Hydrochloric Acid → 5-Formyl-2-isobutoxyphenyl acetate
https://huagongshe.com/reaction/2249690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Hydroxy-4-isobutoxybenzaldehyde | HCID 17816529 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Formyl-2-isobutoxyphenyl acetate | HCID 17816546 | — |
Reaction Steps
In 31 ml of N,N-dimethylformamide are suspended 3.1 g of 3-hydroxy-4-isobutoxybenzaldehyde, 0.7 g of 60% sodium hydride and 3 ml of acetic anhydride. The suspension is stirred for 2 hours at 100° C. The reaction mixture is added to a mixture of ethyl acetate and water, pH is adjusted to 2 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. Thus, 4.2 g of 5-formyl-2-isobutoxyphenyl acetate is obtained as a yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314888B1 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-92a1428cc0b84526b92e2f17daafb34e |
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| Source note | uspto-grants-2008_01 |
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