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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
ReactantBenzyl 2-formylpyrrolidine-1-carboxylateHCID 11064320—
ReactantBenzyl 2-formylpiperidine-1-carboxylateHCID 18375697—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53843982HCID 53843982—
ProductPhenylmethyl 2-(3-ethoxy-3-oxo-1-propen-1-yl)-1-piperidinecarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607951
Source datasetuspto-grants-1997_03
ORD IDord-8bc7f525305d4ef89342b7173215ba4d
Source noteuspto-grants-1997_03