HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861349Generated: October 29, 2026
4-Fluorophenol → (7S,8aS)-7-(4-Fluorophenoxy)methyl-2-(5-cyanophenyl)-1,2,3,4,6,7,8,8 a-octahydro-pyrrolo[1,2-a]pyrazine
https://huagongshe.com/reaction/861349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (7S,8aS)-7-hydroxymethyl-2-(4-cyanophenyl)-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazine | HCID 57229001 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (7S,8aS)-7-(4-Fluorophenoxy)methyl-2-(5-cyanophenyl)-1,2,3,4,6,7,8,8 a-octahydro-pyrrolo[1,2-a]pyrazine | HCID 67648213 | 66% |
Reaction Steps
A solution of 0.25 g (0.97 mmol) of (7S,8aS)-7-hydroxymethyl-2-(4-cyanophenyl)-1,2,3,4,6,7,8,8a-octahydro-pyrrolo[1,2-a]pyrazine (Preparation 16), 0.164 g (1.46 mmol) of 4-fluorophenol, 0.31 g (1.15 mmol) of triphenylphosphine in 10 mL of THF was treated with 0.18 mL (1.15 mmol) of diethyl azodicarboxylate and the solution stirred at ambient temperature for 16 h. The solvent was removed by rotary evaporation, and the residue partitioned between chloroform and 1M sodium hydroxide. The layers were separated, and the organic phase was dried (magnesium sulfate), filtered and evaporated. Purification by flash silica gel chromatography with 1:1 ethyl acetate:hexane gave 0.225 g (66%) of the title compound. mp (.HCl) 81°-85° C. HRMS calcd for C21H23FN3O (MH+): 352.1825, found: 352.1817.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05714487 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-fa9c9f61f32044c98a357e147565c601 |
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| Source note | uspto-grants-1998_02 |
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