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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080549Generated: October 30, 2026

Triphenylphosphine → HCID 86646579, compound

https://huagongshe.com/reaction/2080549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Thiopheneacetic acidHCID 15970—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 86646578HCID 86646578—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86646579HCID 8664657963.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred, cold (0° C.) solution of 3.11 grams (0.012 mole) of triphenylphosphine in 200 mL of THF was added dropwise 2.28 grams (0.011 mole) of diisopropyl azodicarboxylate. The reaction mixture was stirred at 0° C. for five hours and at that time a solution of 1.37 grams (0.0056 mole) of 2-{[(6-chloro(3-pyridyl))methyl](2-methylpropyl)amino}ethan-1-ol and 0.94 gram (0.012 mole) of thiolacetic acid in 50 mL of THF was added dropwise. After complete addition the reaction mixture was stirred at 0° C. for one hour. The reaction mixture was concentrated under reduced pressure to a residue. The residue was purified by column chromatography on silica gel, eluting with mixtures of n-heptane and ethyl acetate. The appropriate fractions were combined and concentrated under reduced pressure, yielding 1.07 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932393B2
Source datasetuspto-grants-2011_04
ORD IDord-d0c315c473f04727bb2d90814df7281d
Source noteuspto-grants-2011_04