HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254467Generated: October 25, 2026
HCID 178491344, compound → HCID 178436445, compound
https://huagongshe.com/reaction/254467
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178491344 | HCID 178491344 | — |
| Reactant | HCID 178506846 | HCID 178506846 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Benzene--cyclohexane (1/1) | HCID 18624872 | — |
| Product | HCID 178436445 | HCID 178436445 | — |
Reaction Steps
To a solution of 10.0 g (38 mmol) [1-(2,6-dimethoxy-phenyl)-meth-(E)-ylidene]-(1-isopropyl-2-methyl-propyl)-amine in 30 ml dry THF cooled to −20° C. were added 91.2 ml of a 0.5M solution of ethyl lithium in cyclohexane/benzene drop-wise to keep temperature below 0° C. Then the mixture was stirred at −20° C. for further 30 min and the reaction quenched by addition of water. The aqueous phase was extracted with ethyl acetate, the combined extracts washed with brine, dried over Na2SO4, filtered and evaporated. Purification of the crude product by flash chromatography on silica gel with a heptane/ethyl acetate gradient provided 4.30 g (E)-[1-(2-ethyl-6-methoxy-phenyl)-methylidene]-(1-isopropyl-2-methyl-propyl)-amine as colourless liquid: MS (EI): 261.4 (M+.), 218.3 ((M-((CH3)2CH)+.), 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875645B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-5f4e6ca46c3041f4a8d66df479d79769 |
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| Source note | uspto-grants-2011_01 |
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