Carbon Tetrachloride → Dimethylthiomalonyl chloride

HRID 1155468Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1155468
[C:1]([Cl:4])(Cl)=[S:2].C(OCC)(=O)C.[CH3:11][C:12]([CH3:15])=[C:13]=[O:14].C(Cl)(Cl)(Cl)[Cl:17]>>[CH3:11][C:12]([CH3:15])([C:13]([Cl:17])=[O:14])[C:1]([Cl:4])=[S:2]

Komponenten

5

Versuchsvorschrift

To a stirred solution of 7.2 ml (9.2 grams, 0.08 mole; 85% in carbon tetrachloride) of thiophosgene in 50 ml of carbon tetrachloride under an argon atmosphere was added dropwise 70.0 grams of an ethyl acetate solution containing 5.6 grams (0.08 mole) of dimethylketene. The addition required five minutes during which time the reaction mixture temperature rose from 25° C. to 32° C. Upon completion of addition the reaction mixture was stirred at ambient temperature for 16 hours. The reaction mixture was concentrated under reduced pressure to a semi-solid residue. The residue was slurried in petroleum ether and a solid collected by filtration. The solid, mp 112°-114° C., was the dimethylketene dimer. The filtrate was concentrated under reduced pressure to a residual oil. The oil was distilled under reduced pressure to give 2.2 grams of dimethylthiomalonyl dichloride; bp 62°-67° C./8-8.5mm. The nmr spectrum was consistent with the assigned structure.

Aufarbeitung

  1. additionThe addition required five minutes during which time the reaction mixture temperature
  2. customrose from 25° C. to 32° C
  3. additionUpon completion of addition the reaction mixture
  4. concentrationThe reaction mixture was concentrated under reduced pressure to a semi-solid residue
  5. filtrationa solid collected by filtration
  6. concentrationThe filtrate was concentrated under reduced pressure to a residual oil
  7. distillationThe oil was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-739643fd81eb4537bc58d3c1d10dd732
Quelldatensatz
uspto-grants-1981_11
Patentnummer
US04302238

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