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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487088Generated: November 1, 2026

(Oxan-4-yl)methanol → HCID 89875911, compound

https://huagongshe.com/reaction/1487088

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Oxan-4-yl)methanolHCID 2773573—
ReactantCyanomethylenetributylphosphoraneHCID 4622928—
Reactantmethyl 5-(N-(4-ethylphenyl)-N-isobutylsulfamoyl)-2-hydroxybenzoateHCID 89875692—
SolventTolueneHCID 1140—
ProductHCID 89875911HCID 89875911—

Reaction Steps

To a solution of (tetrahydro-2H-pyran-4-yl)methanol (74.2 mg, 0.639 mmol) and methyl 5-(N-(4-ethylphenyl)-N-isobutylsulfamoyl)-2-hydroxybenzoate (500 mg, 1.277 mmol) in toluene (0.5 mL) at room temperature, was added a solution of 2-(tributylphosphoranylidene)acetonitrile (339 mg, 1.405 mmol) in toluene (0.5 mL) in one charge. The reaction mixture was stirred vigorously for 1 hour, then left to stand overnight. Additional 2-(tributylphosphoranylidene)acetonitrile (339 mg, 1.405 mmol) and (tetrahydro-2H-pyran-4-yl)methanol (74.2 mg, 0.639 mmol) were added and the reaction mixture stirred for an additional 8 hours. The solvent was evaporated in vacuo to give the crude product, which was purified by silica (Si) chromatography (0-100% ethyl acetate-cyclohexane) to give the title compound as an orange gum, 109.6 mg. LCMS [LCMS1] Rt 1.37 min, m/z (ES+) 490 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428452B2
Source datasetuspto-grants-2016_08
ORD IDord-3dc756ba8b254765a36d441bc51f13aa
Source noteuspto-grants-2016_08