HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034347Generated: October 30, 2026
Acetic Acid → (6-propyl-1,3-benzodioxol-5-yl)methyl acetate
https://huagongshe.com/reaction/1034347
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 67302335 | HCID 67302335 | — |
| Product | (6-propyl-1,3-benzodioxol-5-yl)methyl acetate | HCID 239316 | — |
Reaction Steps
A mixture of dihydrosafrole, 25 g, in acetic acid (25 g) was added, with stirring over 3 hours to a mixture of acetic acid (230 g), paraformaldehyde (45 g) and sulphuric acid (10%, 1.6 g) held at 70° C. After the reaction had been shown to be complete by glc, the excess paraformaldehyde was removed by filtration and the filtrate poured into water (450 ml). Sodium hydroxide solution (20 ml of a 10% solution) was then added. Ether extraction, followed by drying over magnesium sulphate, filtration and evaporation of solvent gave an oil. Methanol (30 ml) was added and after cooling to 0° C. a colourless precipitate of "dimer" (7) was removed by filtration. Evaporation of the filtrate gave 12.7 g of an oil which was purified by distillation to give 7.3 g of colourless oil as 4,5-methylenedioxy-2-propylbenzyl acetate. (b.p. 176°-185° C. at 0.4 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05315018 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-bd3fc655f0a64adfbd80067ed8cb31da |
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| Source note | uspto-grants-1994_05 |
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