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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257394Generated: November 2, 2026

N-(N-tert-Butoxycarbonylpipecolyl)-4-amino-5-benzyloxy-2-oxo-tetrahydrofuran → N-Pipecolyl-4-amino-5-benzyloxy-2-oxotetrahydrofuran

https://huagongshe.com/reaction/2257394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(N-tert-Butoxycarbonylpipecolyl)-4-amino-5-benzyloxy-2-oxo-tetrahydrofuranHCID 22977785—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductN-Pipecolyl-4-amino-5-benzyloxy-2-oxotetrahydrofuranHCID 6675611784.8%

Reaction Steps

N-(N-tert-Butoxycarbonylpipecolyl)-4-amino-5-benzyloxy-2-oxo-tetrahydrofuran (654 mg) was dissolved in 15 ml of 25% trifluoroacetic acid in dichloromethane and stirred at room temperature. The mixture was concentrated to give a gummy residue. The residue was dissolved in dichloromethane and washed with 10% sodium bicarbonate. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to give 422 mg of the title compound as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656627
Source datasetuspto-grants-1997_08
ORD IDord-36b501ff909a4f71ae896813d8a94022
Source noteuspto-grants-1997_08