HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64446Generated: October 29, 2026
Benzyl Alcohol → HCID 131737221, compound
https://huagongshe.com/reaction/64446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | HCID 90072617 | HCID 90072617 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 131737221 | HCID 131737221 | — |
Reaction Steps
To a solution of 340 mg of sodium 2,2-dimethyl-5-(pyridin-2-yl)-1,3-dioxane-5-carboxylate in 5 ml of dioxane and 1 ml of water was added 0.21 ml of isobutyl chloroformate under ice-cooling, followed by stirring for 1 hour. A solution of 850 mg of sodium azide in 3 ml of water was added thereto, followed by stirring for 10 minutes under ice-cooling. To the reaction mixture were added water and diethyl ether to carry out a layer separation operation. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. To the obtained residue was added 5 ml of toluene, followed by stirring at 100° C. for 5 minutes. After leaving to be cooled, 0.7 ml of benzyl alcohol was added thereto at room temperature, followed by stirring at 100° C. for 19 hours. After leaving to be cooled, the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 223 mg of benzyl[2,2-dimethyl-5-(pyridin-2-yl)-1,3-dioxan-5-yl]carbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447090B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-9771d34602b24f909cfe21c6ab6115a5 |
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| Source note | uspto-grants-2016_09 |
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