HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 82922Erstellt: 24. Oktober 2026
Phenol → Tert-butyl 3-phenoxypyrrolidine-1-carboxylate
https://huagongshe.com/reaction/82922
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | 1-Boc-3-pyrrolidinol | HCID 4416939 | — |
| Edukt | Diethyl azodicarboxylate | HCID 5462977 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Tert-butyl 3-phenoxypyrrolidine-1-carboxylate | HCID 23512104 | 25% |
Reaktionsschritte
Phenol (503 mg, 5.34 mmol) and triphenylphosphine (1.40 g, 5.34 mmol) were added to a solution of tert-butyl 3-hydroxypyrrolidine-1-carboxylate (500 mg, 2.67 mmol; which may be prepared as described in Step 1) in anhydrous THF (13 mL) under nitrogen. The reaction mixture was cooled to 0° C. and DEAD (775 μL, 4.27 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated under reduced pressure then diluted with dichloromethane and filtered. The filtrate was washed three times with NaOH 0.2N and brine, dried over Na2SO4 then concentrated. The residue was purified on column chromatography (eluent: pentane EtOAc 9/1) to give the title compound (175 mg, 25%) as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846711B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-4be5dd4fbdd14578b498b174b584f8c4 |
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| Quellennotiz | uspto-grants-2014_09 |
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