HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062506Generated: October 26, 2026
Dichloromethane → 3-(1,3-Dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propyl acetate
https://huagongshe.com/reaction/1062506
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(1,3-Dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propanol | HCID 22281037 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(1,3-Dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propyl acetate | HCID 22281036 | 96% |
Reaction Steps
To a mixture of 15.0 g of 3-(1,3-dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propanol, 9.6 g of acetic anhydride, 100 mg of 4-dimethylaminopyridine and 50 ml of methylene chloride, 10.2 g of triethylamine was added dropwise over 30 minutes at 20° C. Stirring was continued for 30 minutes whereupon 10 g of water was added to stop reaction. Stirring was continued for a further 30 minutes whereupon water was added to the reaction solution, which was extracted with hexane. The organic layer was successively washed with water and saturated sodium chloride water, dried over anhydrous sodium sulfate, and concentrated in vacuum. It was further purified by vacuum distillation, obtaining 16.9 g of 3-(1,3-dioxan-2-yl)-1-(5-norbornen-2-yl)-1-propyl acetate (boiling point 125° C./53 Pa, yield 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06962767B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-ab4caa75d6b04b328cec8aae0bf78847 |
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| Source note | uspto-grants-2005_11 |
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