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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359149Erstellt: 23. Oktober 2026

Dibenzyl sulfide → HCID 15078741, Verbindung

https://huagongshe.com/de/reaction/359149

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibenzyl sulfideHCID 10867—
EduktSodium hydrideHCID 24758—
Eduktalpha,beta-Diphenyl acrylic acidHCID 66677—
EduktMethyl phenylglyoxalateHCID 84835—
EduktThiomandelic acidHCID 10464709—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 15078741HCID 15078741—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To an ice cooled, stirred solution of dibenzyl sulfide (2.14 g, 0.01 m) in dried N,N-dimethylformamide was added sodium hydride (0.88 g, 0.022 mmol of a 60% suspension in mineral oil). The mixture was gradually heated to 60° C. (bath temperature), kept 2 hours and allowed to cool. Methyl benzoylformate (1.42 ml, 0.01 mmol) was then added and the mixture heated at 60° C. for 1 hour, cooled, added to a stirred ice-dilute hydrochloric acid-ether mixture, separated, the aqueous layer re-extracted 1 time with ether, and the combined organic layer washed 2 times with water, dried over sodium sulfate, filtered and concentrated to a residue. Chromatography on silica gel (1 time flush with 10% ethyl acetate/hexane followed by a careful chromatography with a methylene chloride/hexane mixture) yielded 50 mg. of product compound as a pale yellow-white crystalline material. M.S.: M+ =328; NMR: consistent, identical to the nmr spectrum of material prepared from α-phenylcinnamic acid and α-mercaptophenylacetic acid via Michael addition and ring closure. ##STR28##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04999436
Quelldatensatzuspto-grants-1991_03
ORD IDord-97aaa44cbbea4bb3b94f1c2bc649136e
Quellennotizuspto-grants-1991_03