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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73628Generated: October 28, 2026

Cyclohexylamine → HCID 66577520, compound

https://huagongshe.com/reaction/73628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant1-Pentene, 5-bromo-HCID 70704—
Reactant2,4-Dihydropyran-3-oneHCID 11388294—
ReactantButyllithiumHCID 178418339—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66577520HCID 66577520—

Reaction Steps

Cyclohexylamine (3.43 ml, 30.0 mmol) was added to pyran-3-one (3000 mg, 30.0 mmol) in benzene (20 mL). The reaction mixture was stirred at RT for 30 min and then refluxed for 2 hr with a dean-stark trap. The benzene was then distilled off and the residue was redissolved in THF (2 mL) and added to BuLi (13.18 ml, 33.0 mmol) in THF (Volume: 30.000 ml) at 0° C. The reaction mixture was stirred at 0° C. for 1 h before 5-bromo-1-pentene (5582 mg, 37.5 mmol) was added. The reaction mixture was stirred at 0° C. for 2 hr. The mixture was cooled and quenched with water. The reaction mixture was extracted with diethyl ether (3×20 mL). The combined organic fractions were washed with water and brine (saturated, 100 mL), dried, filtered and the solvent was evaporated under reduced pressure (400 mmhg). The residue was purified by column chromatography on silica gel to provide the title compound. 1H NMR (500 MHz, CDCl3) δ 5.74-5.86 (m, 1H), 4.92-5.06 (m, 2H), 3.90-4.06 (m, 3H), 3.77-3.85 (m, 1H), 2.41-2.49 (m, 1H), 2.16-2.24 (m, 1H), 2.01-2.12 (m, 2H), 1.72-1.97 (m, 2H), 1.31-1.49 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829196B2
Source datasetuspto-grants-2014_09
ORD IDord-de77a11043c949ea9b5f52145eb5ae6a
Source noteuspto-grants-2014_09