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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230121Generated: October 28, 2026

Triphenylphosphine → HCID 54162185, compound

https://huagongshe.com/reaction/2230121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Methoxy-5-nitrophenolHCID 69471—
Reactant(2S)-1-Methyl-2-pyrrolidinemethanolHCID 643492—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54162185HCID 5416218589.7%

Reaction Steps

A solution of 2-methoxy-5-nitrophenol (5.58 g; 0.033 mol), (S)-1-methyl-2-hydroxymethylpyrrolidine (3.45 g; 0.03 mol) and triphenylphosphine (8.65 g; 0.033 mol) in dry THF (80 ml) was cooled to 50 and treated with DEAD (5.2 ml; 0.033 mol) over 15 min. The reaction mixture was allowed to stand at RT for 16 h, then evaporated in vacuo and partitioned 5% NaOH(aq)/Et2O. The organic phase was separated and extracted with 10% HCl(aq). The aqueous extract was washed with Et2O, basified with 40% NaOH(aq) and extracted with Et2O. The organic extracts were washed with H2O, dried over Na2SO4 and evaporated in vacuo to yield the title compound (D43) (6.79 g; 85%) MH+=267.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423717B1
Source datasetuspto-grants-2002_07
ORD IDord-cef931ad70124b7d99382fc0334b0e1b
Source noteuspto-grants-2002_07