HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975018Generated: October 29, 2026
Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 53843982, compound
https://huagongshe.com/reaction/975018
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Reactant | Benzyl 2-formylpyrrolidine-1-carboxylate | HCID 11064320 | — |
| Reactant | Benzyl 2-formylpiperidine-1-carboxylate | HCID 18375697 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53843982 | HCID 53843982 | — |
| Product | Phenylmethyl 2-(3-ethoxy-3-oxo-1-propen-1-yl)-1-piperidinecarboxylate | HCID 54132542 | — |
Reaction Steps
To a stirred solution of N-carbobenzyloxypyrrolidine-2-carboxaldehyde or N-carbobenzyloxypiperidine-2-carboxaldehyde (5.00 mmol) [S. Kiyooka, et al., J. Org: Chem., 5409 (1989) and Y. Hamada, et al., Chem. Pharm. Bull., 1921 (1982)] in anhydrous tetrahydrofuran at -78° C. was added (carbethoxymethylene) triphenylphosphorane (2.09 g, 6.00 mmol. 1.2 eq) as a solid portionwise. The resulting reaction mixture was stirred at room temperature under nitrogen for 2 hours, and then heated at reflux under nitrogen for 1 hour. The reaction mixture was evaporated under reduced pressure and the residue was column chromatographed using silica gel (approximately 100 g) and elution with 20% diethyl ether in hexanes afforded either ethyl 3-(N-benzyloxycarbonylpyrrolidin-2-yl)-2-propenoate or ethyl 3-(N-benzyloxycarbonylpiperid-2-yl)-2-propenoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05607951 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-8bc7f525305d4ef89342b7173215ba4d |
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| Source note | uspto-grants-1997_03 |
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