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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriphenylphosphineHCID 11776—
Reactant6-Hydroxy-1,3-benzoxathiol-2-oneHCID 72139—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
SolventTetrahydrofuranHCID 8028—
Product6-Benzyloxy-1,3-benzoxathiol-2-oneHCID 1068262594.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399867B2
Source datasetuspto-grants-2008_07
ORD IDord-1c8230eabd944bb58f2f684305143b62
Source noteuspto-grants-2008_07