HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388698Generated: October 29, 2026
Potassium tert-butoxide → HCID 178437376, compound
https://huagongshe.com/reaction/388698
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 57816686 | HCID 57816686 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178437376 | HCID 178437376 | 73% |
Reaction Steps
Potassium tert-butoxide (2.13 g, 2.2 eq.) was added to a suspension of compound 272 (2.91 g, 1 eq.) in tert-butanol (30 mL). The reaction mixture was heated to 100° C. for 5 hrs. After one night at room temperature, the mixture was diluted with diethyl ether and the precipitate filtered, washed with diethyl ether, and solubilized in water. The pH was adjusted to 6-7 by addition of 1N HCl and the precipitate was filtered, washed with water, and triturated with diethyl ether to yield compound 273 in 73% yield. 1H NMR (CDCl3, 400 MHz): δ (ppm) 4.06 (s, 3H), 5.54 (d, J=10.82 Hz, 1H), 6.25 (d, J=17.31 Hz, 1H), 6.74 (s, 1H), 6.79 (dd, J=17.31 and 10.82 Hz, 1H), 7.06 (d, J=9.10 Hz, 1H), 7.32 (s, 1H), 8.28 (d, J=9.10 Hz, 1H), 9.97 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377962B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-230dcbcd86354547820b0e71da2ede28 |
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| Source note | uspto-grants-2013_02 |
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