HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250410Generated: October 31, 2026
Sodium Hydroxide → 4-(Diphenylmethylene)piperidine
https://huagongshe.com/reaction/2250410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 68905223 | HCID 68905223 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Diphenylmethylene)piperidine | HCID 2762533 | 75.3% |
Reaction Steps
Sodium hydroxide (15.85 g, 396 mmol) in water (30 mL) was added to the carbamate 1-ethoxycarbonyl 4-(diphenylmethylidene)piperidine 19 (11.47 g, 35.7 mmol) dissolved in ethanol (150 mL). The mixture was heated at reflux overnight. The reaction mixture was cooled to room temperature was then partitioned between water (100 mL) and ethyl acetate (150 mL). The mixture was stirred to dissolve the solid and the layers were separated. The organic layer was washed with brine (100 mL) and the separate aqueous layers were extracted with ethyl acetate (100 mL). The combined organic layers were dried with Na2SO4, filtered, and concentrated. The yellow oil was dried by high vacuum to give 6.7 g (75%) of 20 as a yellow-white waxy solid. 1H NMR was used to confirm the structure of the product. (Amine 22 was similarly prepared.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07317026B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-9b6ac1cb3c9448628f842aaa964f58f0 |
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| Source note | uspto-grants-2008_01 |
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