Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394306Generated: October 31, 2026

Triphenylphosphine → 1,1-Dimethylethyl 4-[(1-methyl-1H-tetrazol-5-yl)thio]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1394306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 178482017HCID 178482017—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1,1-Dimethylethyl 4-[(1-methyl-1H-tetrazol-5-yl)thio]-1-piperidinecarboxylateHCID 18539155—

Reaction Steps

To a solution of 1-tert-butoxycarbonyl-4-hydroxypiperidine (1.01 g, 5.0 mmol) in dry THF (30 mL) were added triphenylphosphine (2.0 g, 7.5 mmol) and 5-mercapto-1-methyl-1H-tetrazole (0.70 g, 6.0 mmol). To the mixture was added diisopropyl azodicarboxylate (1.2 mL, 6.0 mmol) under ice cooling, and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was diluted with ethyl acetate (100 mL), which was washed with water, saturated aqueous solution of sodium hydrogen carbonate and saturated aqueous solution of sodium chloride, successively. The solvent was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (50 g, diethyl ether-hexane 1:1) to give the titled compound as a colorless oily substance. (1.11 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348324B2
Source datasetuspto-grants-2008_03
ORD IDord-b78de5c5d6af44348d0dfa0a1dca72a4
Source noteuspto-grants-2008_03