HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2371497Erstellt: 24. Oktober 2026
Hydrochloric Acid → Methyl 2-methyl-3-(4-methylthiobenzyl)inden-1-ylacetate
https://huagongshe.com/de/reaction/2371497
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Iodine | HCID 807 | — |
| Edukt | Methyl bromoacetate | HCID 60984 | — |
| Edukt | 2-Methyl-3-(4-methylthiobenzyl)-1-indanone | HCID 18367456 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Methyl 2-methyl-3-(4-methylthiobenzyl)inden-1-ylacetate | HCID 18367447 | — |
Reaktionsschritte
To a solution of the indanone derivative from Step 1 (885 mg, 3.14 mmol) in ether (20 mL) were added successively zinc (840 mg, 12.8 mmol), methyl bromoacetate (0.5 mL, 5 mmol) and iodine (200 mg). The reaction mixture was refluxed for 3 hours, then cooled to 0° C. and 6N aqueous HCl was added dropwise until the zinc complex was completely decomposed. The organic layer was decanted, washed with brine, dried over Na2SO4 and evaporated to dryness. The oily residue was dissolved in formic acid and evaporated to dryness to complete the dehydration of the intermediate methyl [1-hydroxy-2-methyl-3-(4-methylthiobenzyl)indan-1-yl]acetate. The resulting oily residue was chromatographed on silica gel eluting with a 1:19 mixture of ethyl acetate-hexane to afford pure title compound as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05093356 |
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| Quelldatensatz | uspto-grants-1992_03 |
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| ORD ID | ord-2b2dee6f1c3241459509ee494d9a1377 |
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| Quellennotiz | uspto-grants-1992_03 |
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