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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIodineHCID 807—
EduktMethyl bromoacetateHCID 60984—
Edukt2-Methyl-3-(4-methylthiobenzyl)-1-indanoneHCID 18367456—
KatalysatorZincHCID 23994—
LösungsmittelDiethyl EtherHCID 3283—
ProduktMethyl 2-methyl-3-(4-methylthiobenzyl)inden-1-ylacetateHCID 18367447—

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05093356
Quelldatensatzuspto-grants-1992_03
ORD IDord-2b2dee6f1c3241459509ee494d9a1377
Quellennotizuspto-grants-1992_03