HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971976Generated: October 30, 2026
Potassium Persulfate → HCID 86736116, compound
https://huagongshe.com/reaction/971976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | Potassium Phosphate, Dibasic | HCID 24450 | — |
| Reactant | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| Reactant | HCID 53824762 | HCID 53824762 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86736116 | HCID 86736116 | 77.7% |
Reaction Steps
To a stirred solution of 1.15 g (3.28 mmole) of cis-1-(2,4-dimethoxybenzyl)-2-(2,2-dimethoxyethyl)-3-azido-4-azetidinone in 120 ml of degassed acetonitrile was added at 80°, a solution of 11.8 g (43.7 mmole) of potassium persulfate and 4.05 g (23.3 mmole) of potassium monohydrogenphosphate in 135 ml of degassed water in 6 portions over a 1 hour period. The pH of the mixture was adjusted to 6.5- 7.0 with potassium monohydrogenphosphate after each addition. After one hour, the mixture was cooled to room temperature, the acetonitrile removed in vacuum and the pH adjusted to 8.0. Extraction with ethyl acetate (4× 75 ml) afforded a mixture of product and 2,4-dimethoxybenzaldehyde which was chromatographed over silica gel with benzene-ethyl acetate to give 0.51 g (77%) of the title compound as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04162250 |
|---|
| Source dataset | uspto-grants-1979_07 |
|---|
| ORD ID | ord-91889e1f89a14d589544459a961caaf8 |
|---|
| Source note | uspto-grants-1979_07 |
|---|