HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364246Generated: November 1, 2026
HCID 87212268, compound → HCID 25030275, compound
https://huagongshe.com/reaction/1364246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 87212268 | HCID 87212268 | — |
| Reactant | HCID 178418438 | HCID 178418438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 25030275 | HCID 25030275 | 82.4% |
Reaction Steps
The aldehyde 5 were dissolved in dry THF and cooled to −20° C. thiphen-2-yl magnesium bromide (1.2 eq, 1.651 mM) was then added to the reaction and the reaction was stirred for an additional 2 hrs. After the completion of the reaction as determined by TLC, the reaction mixture was quenched with 0.1 N HCl, followed by washes with saturated sodium bicarbonate solution and brine. The product was purified by flash chromatography using 20% EtOAc/Hexanes as the solvent system to obtain a white solid. Yield=82.4% (Rf=0.26; 20% EtOAc/Hexanes) 1H NMR, 500 MHz Varian, CDCl3, δ 7.31 (d, J=2 Hz, 1H), 7.29 (d, J=4.00 Hz, 1H), 7.12 (d, J=9.50 Hz, 2H), 6.99 (m, J=9.50 Hz, 2H), 6.75 (s, 2H), 6.08 (d, J=4.00, 1H), 3.73 (s, 3H), 2.37 (s, 3H), MS: m/z (ESI, pos.)=333.5 ([M+23])
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888365B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-dd90e2bdf2334d67a2c13c367de1d93e |
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| Source note | uspto-grants-2011_02 |
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