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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493988Generated: October 31, 2026

Tributylphosphine → HCID 67073446, compound

https://huagongshe.com/reaction/493988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantEthyl 5-hydroxy-1H-indole-2-carboxylateHCID 90677—
Reactant(R)-(+)-1-Benzyl-3-pyrrolidinolHCID 643472—
ProductHCID 67073446HCID 6707344649%

Reaction Steps

To a cold (0° C.) mixture of ethyl-5-hydroxyindole-2-carboxylate (purchased at Biosynth, H-6350, 20.5 g, 1.0 eq.), (R)-1-benzyl-3-pyrrolidinol (23 g, 1.3 eq.) and tri-n-butylphosphine (58 mL, 2.0 eq.) was slowly added 1,1′-(azodicarbonyl)dipiperidine (50.4 g, 2.0 eq.) in several portions. The reaction mixture was stirred at room temperature overnight and then filtered off. The filtrate was concentrated in vacuo and diethylether was added. The precipitate was filtered off and the filtrate was concentrated in vacuo and purified on silica eluting with dichloromethane/methanol/ammoniac. One fraction was isolated and dried in vacuo, to yield 18 mg (49%) of the desired product as light yellow foam. MS (m/e): 365.5 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538101B2
Source datasetuspto-grants-2009_05
ORD IDord-d024a6d5e3604913acf95ba2e7876f1d
Source noteuspto-grants-2009_05