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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697Generated: October 25, 2026

Tetrahydrofuran → Methyl 4-[4-sulfonylpyranoyloxy]-2-methoxybenzoate

https://huagongshe.com/reaction/1697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantMethyl 4-hydroxy-2-methoxybenzoateHCID 12532676—
ReactantSulfonylpyran-4-olHCID 19690976—
ProductMethyl 4-[4-sulfonylpyranoyloxy]-2-methoxybenzoateHCID 86752226—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (364 mg, 2.0 mmol) in dry THF (4 mL) was added triphenylphosphine (524.6 mg, 2.0 mmol) and the solution was cooled to 0° C. A 2.5 mL volume of sulfonylpyran-4-ol (200 mg, 1.33 mmol) and diethyl azodicarboxylate (315 μL, 2.0 mmol) in THF was added dropwise via addition funnel over 0.5 h. The reaction was filtered and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column packed in 60:40 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-[4-sulfonylpyranoyloxy]-2-methoxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726172
Source datasetuspto-grants-1998_03
ORD IDord-e3ff06e7d5dc4790a4038ff5d1f041f4
Source noteuspto-grants-1998_03