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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1420742Erstellt: 26. Oktober 2026

Hydrochloric Acid → Methyl 2-methyl-3-(4-methylthiobenzyl)inden-1-ylacetate

https://huagongshe.com/reaction/1420742

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
PatentnummerUS06071934
Quelldatensatzuspto-grants-2000_06
ORD IDord-2d1db58ce95d41b098c5025f4b762663
Quellennotizuspto-grants-2000_06