HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422942Generated: October 31, 2026
Potassium tert-butoxide → HCID 178487799, compound
https://huagongshe.com/reaction/1422942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178487793 | HCID 178487793 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178487799 | HCID 178487799 | — |
Reaction Steps
Potassium tert-butoxide (354 mg, 3.15 mmol, 2.5 eq) is added at room temperature to a stirred solution of [trans-4-(6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthren-3-yl)-cyclohexyl]-carbamic acid tert-butyl ester (2.6 g, 1.26 mmol, 1.0 eq) in dimethyl sulfoxide (45 mL) and tert-butanol (13 mL) under oxygen atmosphere. After 1 hour stirring under oxygen atmosphere, the reaction mixture is purged with nitrogen, and extracted with dichloromethane (3×200 mL) and water (200 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a residue that is purified by column chromatography (silica gel, eluent: dichloromethane:methanol, 250:1 to 100:1, v/v) to afford [trans-4-(4-hydroxy-6-methoxy-3,4-dihydro-2H-1-oxa-9-aza-phenanthren-3-yl)-cyclohexyl]-carbamic acid tert-butyl ester as a white solid that is further purified by preparative HPLC to obtain a white solid (70 mg, 42% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927541B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-4170daf818294bae8f824922cec8e345 |
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| Source note | uspto-grants-2015_01 |
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