HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593725Generated: October 31, 2026
Hydroquinone → (2-Methoxy-2-methyl-1,3-dioxolan-4-yl)methyl prop-2-enoate
https://huagongshe.com/reaction/1593725
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | Glycidol | HCID 11164 | — |
| Reactant | Trimethyl orthoacetate | HCID 15050 | — |
| Product | (2-Methoxy-2-methyl-1,3-dioxolan-4-yl)methyl prop-2-enoate | HCID 17748066 | 56% |
Reaction Steps
47 g of acrylic acid and 3.04 g of p-toluenesulfonic acid were initially charged in a round-bottom flask together with 0.2 g of hydroquinone and heated to 104° C. 40 g of glycidol were added dropwise to this reactant mixture and the resulting solution was stirred at 100° C. for 45 minutes. Subsequently, the reaction mixture was cooled to 25° C. 84 g of trimethyl orthoacetate were added dropwise to this reaction mixture, which was subsequently stirred at 25° C. for one hour. The reaction mixture was then freed of the low boilers present by means of a distillation. Subsequently, a vacuum distillation was carried out at 4 mbar and 95° C. 4-Acryloyloxymethyl-2-methoxy-2-methyl-1,3-dioxolane was obtained in a yield of 56%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07297812B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-538fbce3170148bc80b6d9a69032d7b8 |
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| Source note | uspto-grants-2007_11 |
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