HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403292Generated: November 2, 2026
Benzophenone imine → HCID 86671395, compound
https://huagongshe.com/reaction/2403292
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzophenone imine | HCID 136809 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 71743188 | HCID 71743188 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86671395 | HCID 86671395 | 22% |
Reaction Steps
To a stirred solution of tert-butyl (RS)-2-(6-chloropyridin-3-yl)morpholine-4-carboxylate (1.16 g) and benzophenone imine (977 μl) in toluene (35 ml) was added sodium tert-butoxide (597 mg). The reaction mixture was purged with argon for 10 min. (R)-(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (242 mg) and tris(dibenzylideneacetone)dipalladium(0) (107 mg) were added and the reaction mixture was heated at 100° C. overnight. The reaction mixture was then cooled to room temperature, poured into water and extracted twice with EtOAc. The organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography (silica gel; gradient: 0% to 30% EtOAc in hexanes) to afford tert-butyl (RS)-2-(6-(diphenylmethyleneamino)pyridin-3-yl)morpholine-4-carboxylate (374 mg, 22%) as a yellow oil. MS (ISP): 444.2 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802673B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-bf54d4f69b494617903f0a70b0055824 |
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| Source note | uspto-grants-2014_08 |
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