HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106700Generated: October 31, 2026
HCID 10956231, compound → HCID 53857488, compound
https://huagongshe.com/reaction/1106700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10956231 | HCID 10956231 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 131721786 | HCID 131721786 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53857488 | HCID 53857488 | 96.6% |
Reaction Steps
The product from Step C (2.07 g) was dissolved in 10 mL of tetrahydrofuran and 10 mL of 1.0 M potassium t-butoxide in THF was added dropwise. After the addition was complete, the mixture was stirred 15 min, and then the title compound of Step E (2.06 g) was added. The reaction mixture was stirred at room temperature overnight, and then diluted with 20 mL of water and extracted with three 30 mL portions of ethyl acetate. The combined organic extracts were dried (MgSO4), filtered, and concentrated to give 3.53 g of the title compound of Step F as an oil. 1H NMR (CDCl3): δ 7.5 (m,5H), 7.25 (m,2H), 5.34 (d,1H), 5.18 (d,1H), 3.49 (s,3H), 2.08 (s,3H). The crude product contained minor amounts of impurities and solvent, but the material was not further purified before Step G.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057352 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-f27fe34a26874a9e84fb928a576864a4 |
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| Source note | uspto-grants-2000_05 |
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