HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415572Generated: October 26, 2026
HCID 59402704, compound → HCID 59402815, compound
https://huagongshe.com/reaction/415572
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59402704 | HCID 59402704 | — |
| Reactant | HCID 178511344 | HCID 178511344 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 59402815 | HCID 59402815 | 13% |
Reaction Steps
(Method F) Lithium acetylide ethylenediamine complex (305 mg, 3.3 mmol, 1.1 equiv.) was placed in a three-neck flask, degassed, flushed with N2 and suspended in DMSO (2 ml). To the stirred suspension a solution of 3-[(7-bromoheptyl)oxy]benzenecarboxamide (943 mg, 3 mmol, 1 equiv.) in DMSO (2 ml), was added, slowly, dropwise, at r.t., under N2. The reaction mixture was stirred at r.t. for 16 h. After that time it was diluted with 1N HCl solution and extracted with EtOAc (×3). The combined organic extracts were washed with brine, dried (Na2SO4) and evaporated to dryness under reduced pressure. The crude product was purified by column chromatography on silica eluting with EtOAc/hexane 20%, to give the desired compound as a white solid (100 mg, 13%), mp 82-83° C. HPLC-MS (method 1): m/z 260 [M+H]+, Rt=4.26 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088791B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-96c57823b09740ee8ff7c988750df4a6 |
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| Source note | uspto-grants-2012_01 |
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