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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Oxan-4-yl)methanol | HCID 2773573 | — |
| Reactant | Cyanomethylenetributylphosphorane | HCID 4622928 | — |
| Reactant | methyl 5-(N-(4-ethylphenyl)-N-isobutylsulfamoyl)-2-hydroxybenzoate | HCID 89875692 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 89875911 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428452B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-3dc756ba8b254765a36d441bc51f13aa |
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| Source note | uspto-grants-2016_08 |
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