HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416596Generated: October 30, 2026
Triphenylphosphine → HCID 54565828, compound
https://huagongshe.com/reaction/1416596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Methyl-5-hydroxypyridine | HCID 14275 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (S)-(-)-N-Boc-prolinol | HCID 643448 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54565828 | HCID 54565828 | 57% |
Reaction Steps
To a solution of triphenylphosphine (3.83 g, 14.60 mmol) in 40 mL of anhydrous THF at 0° C. was added diethyl azodicarboxylate (2.3 mL, 14.60 mmol) dropwise. The mixture was stirred at 0° C. for 30 minutes, then brought to room temperature. (S)-1-t-Butoxycarbonyl-2-pyrrolidinemethanol (1.96 g, 9.75 mmol, Aldrich Chemical Co.) and 6-methyl-3-pyridinol (Aldrich Chemical Co.,1.60 g, 14.60 mmol) were added to the reaction vessel, and the mixture was stirred for 16 hours. Solvent was removed in vacuo, and the residue was diluted with hexane and sonicated for 30 minutes. The resulting precipitate was filtered and washed with hexane. The hexane was removed in vacuo. The residue was purified by silica gel flash chromatography using a gradient from 100% hexane to a 1:1 solution of ethyl acetate/hexane (100% Hex, 10%EtOAc/Hex, 20%EtOAc/Hex, 1:1 EtOAc/Hex) to give 1.61 g (57%) of the title compound as a pale yellow oil. TLC Rf=0.42 (1:1 EtOAc/Hex). MS (DCI/NH3) m/e: 293 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05914328 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-5deba47e48574699aac2a63145c99054 |
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| Source note | uspto-grants-1999_06 |
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