HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240432Generated: October 31, 2026
Potassium tert-butoxide → HCID 86680443, compound
https://huagongshe.com/reaction/240432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 89466305 | HCID 89466305 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86680443 | HCID 86680443 | — |
Reaction Steps
To a solution of Example 35E (8 g, 0.023 mol) in methanol (25 mL) was added potassium t-butoxide (14.5 g, 0.129 mol), and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated, the residue was diluted with 5% citric acid in water (100 mL), and the mixture was extracted with ethyl acetate (50 mL×2). The combined organic layers were discarded. The aqueous layer was basified using K2CO3 to pH 8-9 and extracted with ethyl acetate (50 mL×2). The combined organic layers were dried over Na2SO4 and concentrated to give the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 1.48 (s, 9H), 1.56-1.69 (m, 1H), 1.86-1.97 (m, 1H), 2.10-2.35 (m, 3H), 2.35-2.48 (m, 1H), 2.52-2.72 (m, 1H), 2.78-2.97 (m, 2H), 3.03 (dt, 1H, J=17.1, 2.4 Hz), 3.92-4.15 (m, 2H), 4.32 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648074B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-1e82b89d1ea04a2098b40f1f25985131 |
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| Source note | uspto-grants-2014_02 |
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