HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1292504Erstellt: 25. Oktober 2026
Ethyl Bromide → 4-Methoxyimino-5-methyl-6-bromothiochroman
https://huagongshe.com/reaction/1292504
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Bromide | HCID 6332 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | 4-Methoxyimino-5-methyl-6-(1-ethyl-5-n-propanesulfonyloxypyrazol-4-yl)-carbonylthiochroman-1,1-dioxide | HCID 86752664 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Methoxyimino-5-methyl-6-bromothiochroman | HCID 54382502 | — |
Reaktionsschritte
1.1 Grams (46 mmol) of magnesium was dispersed in 10 ml of THF, and 2.2 g (20 mmol) of ethyl bromide was dropwise added under nitrogen current. The mixture was allowed to react for 10 minutes, and then a THF solution of 2.9 g (10 mmol) of the 4-methoxyimino-5-methyl-6-bromothiochroman obtained in the above (1) was gradually added at room temperature. The mixture was refluxed for 3 hours and then cooled to room temperature, and carbon dioxide gas was bubbled in for 1 hour. To the reaction mixture was added 5% hydrochloric acid, and the mixture was extracted with ether. An ether layer was extracted with a 5% potassium carbonate aqueous solution, and an aqueous layer was neutralized with concentrated hydrochloric acid. The neutralization product was extracted with ethyl acetate, and the extract was washed with a saturated sodium chloride aqueous solution. The washed extract was dried over sodium sulfate, and then the solvent was distilled off to give 1.6 g (yield 63%) of 4-methoxyimino-5-methylthiochroman-6-carboxylic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05756759 |
|---|
| Quelldatensatz | uspto-grants-1998_05 |
|---|
| ORD ID | ord-6af1fb0950344ef19641359dc4c23735 |
|---|
| Quellennotiz | uspto-grants-1998_05 |
|---|