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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424437Generated: October 30, 2026

Triphenylphosphine → HCID 66703997, compound

https://huagongshe.com/reaction/424437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Bromo-1-propanolHCID 12308—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantHCID 66703958HCID 66703958—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66703997HCID 66703997100%

Reaction Steps

Diisopropyl azodicarboxylate (40% in toluene, 13.6 g, 26.9 mmol) was added to a solution of tert-butyl (2S)-2-(4-hydroxyphenyl)morpholine-4-carboxylate (5.0 g, 17.9 mmol), triphenylphosphine (7.1 g, 27.1 mmol) and 3-bromopropanol (3.75 g, 27.0 mmol) in tetrahydrofuran (100 ml) and the solution was stirred for 10 hours at room temperature. The mixture was partitioned between water and ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography eluting 5-10% methanol in chloroform to furnish tert-butyl (2S)-2-(4-(3-bromopropyloxy)phenyl)morpholine-4-carboxylate (7.16 g, 100%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106045B2
Source datasetuspto-grants-2012_01
ORD IDord-13042097aeaa4f78b0f7a3aff50d842f
Source noteuspto-grants-2012_01