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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116604Generated: October 30, 2026

Tributylphosphine → HCID 11371308, compound

https://huagongshe.com/reaction/2116604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 67418417HCID 67418417—
Reactant7-HydroxyquinolineHCID 135426866—
SolventAmmoniaHCID 222—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
ProductHCID 11371308HCID 1137130848.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.26 g (1.03 mmol) of 1,1′-(azodicarbonyl)-dipiperidine (ADDP) is added to a solution of 0.16 g (0.69 mmol) of 2-(methyloxy)-2-oxoethyl 4-(hydroxymethyl)-1-piperidinecarboxylate, prepared in Step 8.1., 0.26 ml (1.03 mmol) of tri-n-butylphosphine and 0.13 g (0.90 mmol) of 7-hydroxyquinoline in 2.5 ml of benzene, which is cooled by means of an ice bath. The mixture is stirred at 0° C. for 15 minutes and then at ambient temperature for 16 hours. It is filtered over celite and rinsed with diethyl ether. The filtrates are evaporated to dryness and purified by chromatography on silica gel, eluting with a 70/30 mixture of ethyl acetate in n-hexane. The product obtained is dissolved in 3 ml (21 mmol) of a 7M solution of ammonia in methanol. The solution is stirred for 3 hours and then evaporated to dryness. The product is purified by chromatography on silica gel, eluting with a 90/10 mixture of ethyl acetate in ethanol, and recrystallized from ethyl acetate, to give 0.115 g of product in white solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439257B2
Source datasetuspto-grants-2008_10
ORD IDord-47ee2433451b480d977a37946fb5c8a4
Source noteuspto-grants-2008_10