HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582133Generated: October 25, 2026
N-methoxy-N-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)prop-2-enamide → HCID 21193738, compound
https://huagongshe.com/reaction/582133
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methoxy-N-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)prop-2-enamide | HCID 54075299 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21193738 | HCID 21193738 | 97% |
Reaction Steps
To a stirred solution of N-methoxy-N-methyl-3-(3-cyclopentyloxy-4-methoxyphenyl)prop-2-enamide (1.986 g, 6.50 mmol) in dry tetrahydrofuran (15 ml) at -78° C. was added methyl lithium (1.4M solution in hexanes, 10.20 ml, 14.3 mmol) dropwise over 3 minutes. The resulting solution was stirred for 1 hour at 0° C., after which time the reaction mixture was diluted with 5% HCl in methanol (20 ml) at 0° C., and partitioned between brine (35 ml) and an equal volume of methylene chloride and diethyl ether (100 ml). The organics were dried (Na2SO4) and concentrated in vacuo to give a light yellow oil. The oil was purified by flash chromatography (SiO2 ; ethyl acetate/hexane (35:65)) to afford the title compound as a colorless oil (1.642 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922751 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-04ec3b1e33d446ce8d1f98da301597c4 |
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| Source note | uspto-grants-1999_07 |
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