HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748890Generated: October 28, 2026
Benzyl Alcohol → 6-Benzyloxy-1,3-benzoxathiol-2-one
https://huagongshe.com/reaction/748890
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 6-Hydroxy-1,3-benzoxathiol-2-one | HCID 72139 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Benzyloxy-1,3-benzoxathiol-2-one | HCID 10682625 | 94.2% |
Reaction Steps
Dissolve 6-hydroxy-1,3-benzoxathiol-2-one (16.8 g, 0.1 mol) in THF (1650 mL) and cool to 0° C. Sequentially add benzyl alcohol (16.2 g, 0.15 mol), triphenylphosphine (PPh3, 39.3 g, 0.15 mol), and diisopropylazodicarboxylate (30.3 g, 0.15 mol). Stir the reaction mixture at room temperature overnight. Add water (1500 mL) and extract the aqueous layer with EtOAc (3×1500 mL). Combine the organic layers and dry with Na2SO4, filter, concentrate and purify by flash column chromatography (silica gel, 10-25% of EtOAc/hexane) to give 24.33 g of 6-benzyloxy-benzo[1,3]oxathiol-2-one (94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399867B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-1c8230eabd944bb58f2f684305143b62 |
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| Source note | uspto-grants-2008_07 |
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