HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877942Generated: October 30, 2026
Sodium Acetate → ethyl 2-((4R,6S)-6-(acetoxymethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate
https://huagongshe.com/reaction/877942
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | ethyl 2-((4R,6S)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate | HCID 67323517 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | ethyl 2-((4R,6S)-6-(acetoxymethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate | HCID 53339171 | — |
Reaction Steps
Mixture of ethyl 2-((4R,6S)-6-(chloromethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate (60 grams), tetra butyl ammonium bromide (79 grams) and anhydrous sodium acetate (61.2 grams) was heated to reflux temperature and stirred. After the completion of the reaction, the reaction mixture was cooled to 25-30° C. and petroleum ether (50 ml) was added to it then stirred for 60 minutes at 25-30° C. The reaction mixture was filtered and washed with petroleum ether. The solvent from the filtrate was distilled off under reduced pressure to get the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987444B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-39710b81b78c4c13afa29ee5dc0b9e9e |
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| Source note | uspto-grants-2015_03 |
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