HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782042Generated: October 30, 2026
Water → 1'-Benzyl-3H-spiro[2-benzofuran-1,4'-piperidine]
https://huagongshe.com/reaction/1782042
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Benzyl-4-(2-hydroxymethyl-phenyl)-piperidin-4-ol | HCID 12289669 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1'-Benzyl-3H-spiro[2-benzofuran-1,4'-piperidine] | HCID 12213003 | 94.7% |
Reaction Steps
Crude 1-benzyl-4-(2-hydroxymethyl-phenyl)-piperidin-4-ol (180 g, 0.605 mol) was dissolved in THF (1000 mL). Triethylamine (176.18 mL, 1.27 mol) was added. A solution of methanesulfonyl chloride (33.03 mL, 0.424 mol) in THF (100 mL) was added slowly which caused an increase of the temperature from ambient to 53° C. The reaction was then refluxed for 4 h. Water (500 mL) and AcOEt (500 mL) were added to the reaction mixture. The organic phase was separated, dried and evaporated to give a brown oil (160 g).The crude product was purified by chromatography on silica gel with heptane/AcOEt 100:0 to 60:40 to give a light yellow solid (120 g, 71%). MS: m/z=280 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07498339B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-c6ed65c4c5784155ae2a68b08100f3ea |
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| Source note | uspto-grants-2009_03 |
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