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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1390841Erstellt: 26. Oktober 2026

Hydrochloric Acid → Alpha-amino-6-chloro-3-indoleacrylic acid methylester hydrochloride

https://huagongshe.com/reaction/1390841

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethanolHCID 887—
EduktAlphanitro-6-chloro-3-indoleacrylic acid methylesterHCID 53746644—
LösungsmittelDiethyl EtherHCID 3283—
ProduktAlpha-amino-6-chloro-3-indoleacrylic acid methylester hydrochlorideHCID 70550909180,1%

Reaktionsschritte

A 3-l. three-necked flask, equipped with a thermometer and a mechanical stirrer was charged with 316 g (1.4 moles) of stannous chloride dihydrate and a solution of 111 g (3 moles) of dry hydrogen chloride gas in 1 l. of methyl alcohol. The colorless solution was stirred and cooled to -30° in a dry ice-acetone bath. 112.3 g (0.40 moles) of alpha-nitro-6-chloro-3-indoleacrylic acid methylester was added in 4 equal portions over 1 hour, maintaining the temperature between -25 and -20°. After the addition was complete, the temperature was allowed to rise to -10° and stirring at this temperature was continued for 90 minutes. Then 500 ml. of ether was added to the yellow suspension, followed by addition of 500 ml of 12N hydrochloric acid (concentrated), the temperature was kept below 5°. The mixture was then filtered through a Buchner funnel. The filter cake was washed with 1000 ml of methyl alcohol-9N aqueous hydrochloric acid 1:1, precooled to -20°, and 400 ml of ether. The tan product was dried at 40°/0.1 mmHg for 8 hours and then at 20°/0.1 mmHg to constant weight to yield 103.4 g (90%) of crude product, m.p. 191° (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04140697
Quelldatensatzuspto-grants-1979_02
ORD IDord-1371b11e56b84597954a8862872a05ea
Quellennotizuspto-grants-1979_02