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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173902Generated: October 30, 2026

Toluene → HCID 86701437, compound

https://huagongshe.com/reaction/2173902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTributylphosphineHCID 13831—
Reactantbenzyl N-(2-hydroxyethyl)carbamateHCID 280458—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactanttert-Butyl 3-(3-hydroxyphenyl)piperazine-1-carboxylateHCID 16740841—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86701437HCID 86701437—

Reaction Conditions

Temperature0 °C

Reaction Steps

(+) or (−)-tert-butyl 3-(3-hydroxyphenyl)piperazine-1-carboxylate (tr=9.7 min) (Biological Example 2.1) (300 mg, 1.078 mmol) and benzyl 2-hydroxyethylcarbamate (210 mg, 1.078 mmol) were dissolved in THF (10 ml). Tributylphosphine (0.404 ml, 1.617 mmol) was added, and after cooling to 0° C., DEAD 40% in toluene (0.640 ml, 1.617 mmol) was added dropwise. The reaction was stirred for 2 h at 0° C., then overnight at rt. The reaction mixture was diluted with aqueous NaHCO3. The layers were separated and the aqueous layer was extracted with AcOEt. The organic phase dried over MgSO4 and concentrated in vacuum. The crude residue was purified by preparative HPLC (Macherey-Nagel Nucleosil 100-10 C18, CH3CN/H2O (0.1% TFA)) to give the title compound. MS (ESI+) m/z 455.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056874B2
Source datasetuspto-grants-2015_06
ORD IDord-36dea08cbee04e1c926400742e09417b
Source noteuspto-grants-2015_06