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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942448Generated: November 2, 2026

Triphenylphosphine → HCID 67330598, compound

https://huagongshe.com/reaction/1942448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBenzoic acid, 4-hydroxy-3-nitro-, methyl esterHCID 66835—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(L)-ethyl lactateHCID 92831—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67330598HCID 67330598—

Reaction Steps

To a solution of methyl 4-hydroxy-3-nitrobenzoate (5.0 g) and ethyl L-lactate (2.9 ml) in tetrahydrofuran (120 ml) was added triphenylphosphine (10 g), and the mixture was stirred at room temperature for 10 minutes. To the mixture was added under ice-cooling diisopropyl azodicarboxylate (20 ml), and the mixture was stirred at 60° C. for 4 hours. The reaction solution was cooled to room temperature, and water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=5/1) to give the title compound (9.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-5e50d3d924e248c0956dc57732889bc5
Source noteuspto-grants-2013_03