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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400235Generated: October 26, 2026

N,N,N',N'-Tetramethylazodicarboxamide → Triphenylphosphine Oxide

https://huagongshe.com/reaction/400235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylazodicarboxamideHCID 4278—
ReactantCarbon TetrachlorideHCID 5943—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropylethylamineHCID 81531—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductTriphenylphosphine OxideHCID 13097—
ProductOxazolineHCID 68157—

Reaction Steps

Triphenylphosphine (654 mg, 2.46 mmol) was added to a stirred solution of diamide F (400 mg, 0.75 mmol) in acetonitrile (15 mL). After a few minutes, N,N-diisopropylethyl amine (440 μl, 2.52 mmol) was added. Addition of carbon tetrachloride (800 μl) followed. The mixture was stirred for 24 hours, diluted with ethyl acetate (100 mL) and washed with aqueous sodium bicarbonate solution and brine. The organic extract was dried (magnesium sulfate), filtered and concentrated. The residue was chromatographed on a silica gel column and eluted with 50% ethyl acetate in hexanes, followed by ethyl acetate and 2-5% methanol in ethyl acetate to obtain oxazoline G (450 mg, contaminated with triphenylphosphine oxide) as a mixture of diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05827868
Source datasetuspto-grants-1998_10
ORD IDord-d86487837e574210b2cf97c5816a36ea
Source noteuspto-grants-1998_10