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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442462Generated: November 1, 2026

Benzene → HCID 57315705, compound

https://huagongshe.com/reaction/442462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantDiethyl chlorophosphateHCID 13139—
Reactanttert-Butyl isocyanoacetateHCID 2759404—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductHCID 57315705HCID 57315705—

Reaction Steps

1 ml of an approximately 2 molar solution of butyllithium in hexane is added over a period of 15 minutes to a solution, cooled to -10° C., of 282 mg (2 mmols) of isocyanoacetic acid tert.-butyl ester in 3 ml of dry hexane (distilled over sodium), whilst stirring vigorously and in a nitrogen atmosphere. The suspension which forms is stirred for a further 10 minutes and a solution of 413 μl (2 mmols) of diethyl phosphorochloridate in 5 ml of dry hexane is then added over a period of 15 minutes. The reaction mixture is stirred for a further 30 minutes, then treated with 20 ml of benzene and 5 ml of water and stirred vigorously for a further 10 minutes. The organic phase is washed with 3 times 5 ml of saturated aqueous sodium chloride solution, dried over sodium sulphate and evaporated in vacuo. The residue is chromatographed on silica gel. Benzene/ethyl acetate, 3:1, elutes diethylphosphono-isocyanoacetic acid tert.-butyl ester as a pale yellow oil; IR spectrum (in methylene chloride): characteristic bands at 3.4; 4.64; 5.70; 7.30; 8.00; 8.70 and 9.80μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045520
Source datasetuspto-grants-1977_08
ORD IDord-d1598b234bdc4ceda7ce8db8a4285bdc
Source noteuspto-grants-1977_08