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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-Benzyl-4-(2-hydroxymethyl-phenyl)-piperidin-4-olHCID 12289669—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1'-Benzyl-3H-spiro[2-benzofuran-1,4'-piperidine]HCID 1221300394.7%

Reaction Conditions

Temperature53 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498339B2
Source datasetuspto-grants-2009_03
ORD IDord-c6ed65c4c5784155ae2a68b08100f3ea
Source noteuspto-grants-2009_03