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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790642Generated: November 1, 2026

Triphenylphosphine → HCID 11616105, compound

https://huagongshe.com/reaction/1790642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 11638054HCID 11638054—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11616105HCID 11616105—

Reaction Conditions

Temperature45 °C

Reaction Steps

Triphenylphosphine (0.25 g, 0.952 mmol) was added to a solution of (2R,5S,6S)-5-azido-6-hydroxy-2-methyl-azepane-1-carboxylic acid benzyl ester (0.193 g, 0.635 mmol) in THF (10 ml) and H2O (0.04 ml), then was heated to 45 degrees C. overnight. The reaction mixture was then diluted with toluene (100 ml×2) and was azeotroped in vacuo by rotary evaporation twice. The resulting oil was dissolved in MeOH and HCl in Et2O and the resulting salt was collected following filtration and was used in the next reaction without further purification (0.27 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071184B2
Source datasetuspto-grants-2006_07
ORD IDord-16fdd40419f0425e98a3f5ddf212111d
Source noteuspto-grants-2006_07