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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376832Generated: October 31, 2026

4-Nitrobenzaldehyde → HCID 22916912, compound

https://huagongshe.com/reaction/1376832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantWaterHCID 962—
Reactant1,1-Dimethylethyl dichloroacetateHCID 3016483—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22916912HCID 2291691271.6%

Reaction Steps

5.55 g of tert.-butyl dichloroacetate in 30 ml of tetrahydrofuran and 4.99 g of 4-nitrobenzaldehyde in 30 ml of tetrahydrofuran were cooled to -20° C. and, over 20 minutes, 30 ml of a molar solution of potassium tert.-butylate in tetrahydrofuran were added dropwise at -20° C. The reaction mixture was stirred while the temperature was allowed to rise to 20° C., and it was then poured into 100 ml of water and ice, and was extracted with ether. The organic phase was washed with water saturated with sodium chloride, then with water, dried, and concentrated to dryness under reduced pressure. The residue was chromatographed on silica and eluted with methylene chloride to obtain 6.44 g of 1,1-dimethylethyl 2-chloro-3-(4-nitrophenyl)oxirane carboxylate melting at 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663164
Source datasetuspto-grants-1997_09
ORD IDord-60fadf5be787429aab729c8f5afc0d3d
Source noteuspto-grants-1997_09