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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068174Generated: November 1, 2026

p-Toluenesulfonic acid → (5S)-4-Methyl-4-azaspiro[2.4]heptane-5-methanol

https://huagongshe.com/reaction/2068174

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 67296569HCID 67296569—
SolventMethanolHCID 887—
Product(5S)-4-Methyl-4-azaspiro[2.4]heptane-5-methanolHCID 6729666880%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of (5S)-4-methyl-5-((tetrahydro-2H-pyran-2-yloxy)methyl)-4-azaspiro[2.4]heptane (64 mg, 0.284 mmol) in 10 mL of methanol was added 4-methyl-benzenesulfonic acid (97.8 mg, 0.568 mmol, Aldrich). The reaction mixture was stirred at 50° C. overnight, and then concentrated in vacuo. The residue was treated with 10 mL of saturated Na2CO3 aqueous solution, and extracted with dichloromethane (20 mL×3). The combined organic phases were dried over Na2SO4 and concentrated in vacuo to give the desired product as yellow oil (32 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293897B2
Source datasetuspto-grants-2012_10
ORD IDord-d1eac4a2daf4457c91ec9a3999bf16bb
Source noteuspto-grants-2012_10