HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406790Generated: October 30, 2026
Sodium t-butoxide → HCID 74788457, compound
https://huagongshe.com/reaction/406790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 74788459 | HCID 74788459 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 74788457 | HCID 74788457 | 94% |
Reaction Steps
A solution of compound 16 (127 mg, 0.304 mmol) in MeOH (1 mL) was treated with NaOtBu (146 mg, 1.52 mmol) at 0° C. After stirring at rt for 4 h, the reaction was quenched adding sat. NH4Cl (2 mL) and extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by flash chromatography using gradient elution from 0% EtOAc-hexane to 30% EtOAc-hexane to afford the title compound as a thick oil (95 mg, 94% yield). 1H NMR (400 MHz, CDCl3) δ 6.68-6.60 (m, 2 H), 6.48-6.44 (m, 2 H), 5.48 (bs, 1H), 3.94-3.90 (m, 1 H), 3.70-3.65 (m, 2 H), 2.64-2.60 (m, 1 H), 1.84-1.81 (m, 1 H), 1.45-1.39 (m, 10 H), 0.98-0.95 (m, 2 H), 0.76-0.73 (m, 1 H), 6.64-6.62 (m, 2 H), 0.35-0.34 (m, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754132B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-66bb232d1d6b4867a7e4586f19ef8007 |
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| Source note | uspto-grants-2014_06 |
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