HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376832Generated: October 31, 2026
4-Nitrobenzaldehyde → HCID 22916912, compound
https://huagongshe.com/reaction/1376832
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1,1-Dimethylethyl dichloroacetate | HCID 3016483 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22916912 | HCID 22916912 | 71.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663164 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-60fadf5be787429aab729c8f5afc0d3d |
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| Source note | uspto-grants-1997_09 |
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