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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271499Generated: November 1, 2026

Triphenylphosphine → HCID 86722610, compound

https://huagongshe.com/reaction/2271499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant1-Azetidinecarboxylic acid, 3-[(3,4-dichlorophenyl)hydroxymethyl]-, 1,1-dimethylethyl esterHCID 59446741—
ReactantHCID 178418441HCID 178418441—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86722610HCID 8672261088%

Reaction Conditions

Temperature0 °C

Reaction Steps

Tetrazole (90.0 mg, 1.28 mmol) was added to tertiary butyl 3-((3,4-dichlorophenyl)(hydroxy)methyl)azetidine-1-carboxylate (200 mg, 0.638 mmol) and triphenylphosphine (335 mg, 1.28 mmol) dissolved in the distilled tetrahydrofuran solution (15.0 mL), and diisopropyl azocarboxylate (0.25 mL, 1.28 mmol) was slowly added thereto at 0° C., and the mixture was stirred at room temperature for one day. The solvent of the reaction mixture was removed by reduced pressure evaporation to obtain a yellow liquid, which was purified by flash chromatography (n-hexane:ethyl acetate (4:1, v/v)). The product was identified as a single compound by TLC (n-hexane:ethyl acetate (4:1, v/v)) (yield: 88%, white solid). This white solid was dissolved in 10 mL of methanol solution, and 1 N HCl (3.0 mL) was added thereto, and heated to reflux at 60° C. for one day. Thereafter, the solvent of the reaction mixture was removed by reduced pressure evaporation to obtain the title compound (KHG27280).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120771B2
Source datasetuspto-grants-2015_09
ORD IDord-8a41be24fdcf4e57a2c0c6a2848c75fe
Source noteuspto-grants-2015_09