HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278018Generated: November 2, 2026
Benzyl Alcohol → {6-[(Benzyloxy)methyl]-1,4-dioxan-2-yl}methanol
https://huagongshe.com/reaction/1278018
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Diglycidyl ether | HCID 16704 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Product | {6-[(Benzyloxy)methyl]-1,4-dioxan-2-yl}methanol | HCID 54004886 | 20.1% |
Reaction Steps
108 g of benzyl alcohol (1.0 mole) is stirred under a nitrogen atmosphere at room temperature and 0.4 g of sodium is added to the mixture and stirring continued for 2-1/2 hours. Then 13.1 g of 2,2'-(oxybismethylene)bisoxirane (0.1 mole) is added and the mixture then heated to reflux for 18 hours. The mixture is then cooled to room temperature and with stirring is poured into 350 ml of water. The aqueous mixture is extracted with 2×200 ml portions of chloroform, the CHCl3 extracts are combined and dried over anhydrous sodium sulfate. The CHCl3 is removed in vacuo and the resulting yellow oil then vacuum distilled through a 10 cm vigreux column. The fraction distilling at 150°-154° @0.4 mm is collected yielding 4.8 g (20%) of the above compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04279902 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-bdfb172dd63344a1a76e90c60281b246 |
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| Source note | uspto-grants-1981_07 |
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