Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377937Generated: October 31, 2026

Triphenylphosphine → HCID 10872275, compound

https://huagongshe.com/reaction/1377937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 131720187HCID 131720187—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10872275HCID 1087227551%

Reaction Steps

1.05 grams (S)-Acetic acid [[6-[2-[hydroxy]propyl]-1,3-benzodioxol-5-yl](4-nitrophenyl)methylene]hydrazide and 0.78 grams triphenylphosphine in 70 mL tetrahydrofuran were cooled to 0° C. 0.57 grams diethyl azodicarboxylate in 5 mL tetrahydro-furan was added dropwise over 15 min. The resulting mixture was stirred for 2 h then warmed to room temperature for 2 h. The mixture was transferred to a separatory funnel and the solution was washed with 1N HCl, water and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated by rotary evaporation. The residue was eluted through a silica gel column (1:1 ethyl acetate:hexane). Fractions containing the desired compound were concentrated to a yellow oil which solidified on standing. The yellow crystalline material was slurried in 30 mL of CH2Cl2 and hexane (3:7) at 0° C. The precipitate was removed by filtration and the filtrate was concentrated to a yellow foam. The residue was suspended in 10 mL ethanol which was warmed to reflux then slowly cooled to room temperature. The precipitate was collected by filtration and dried in a vacuum oven at 60° C. to give 0.51 grams (50%) of the subtitled product (100% ee) which was 98.3% pure by HPLC potency assay.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665878
Source datasetuspto-grants-1997_09
ORD IDord-4055a27435f34188ac02108b81dc0bc9
Source noteuspto-grants-1997_09