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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 516429Erstellt: 24. Oktober 2026

Sodium Hydroxide → 5-Methyl-6-oxoheptanesulfonic acid

https://huagongshe.com/de/reaction/516429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acidHCID 58084006—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt5-Methyl-6-oxoheptanesulfonic acidHCID 57903351—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of 290 mg of NaOH in 3 ml water was added to the mixture of 710 mg (2.53 mmol) of 5-ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acid in 15 ml of methanol. The obtained mixture was stirred for 15 hours at 50° C. Methanol was removed by a rotary evaporator, residue was acidified to pH 1 and then solvent was removed until dry to yield 5-methyl-6-oxo-1-heptanesulfonic acid. The product thus obtained (940 mg, 4.5 mmol), 1.02 g (5.4 mmol) of 4-hydrazinobenzenesulfonic acid, and 15 ml of acetic acid was refluxing for 16 hours. The insoluble precipitate was filtered and the filtrate was evaporated. The obtained residue was column purified (RP-18, water) to yield 840 mg of the 2,3-dimethyl-3-(4-sulfobutyl)-3H-5-indolesulfonic acid (IVd). δH (200 MHz, DMSO-d6): 7.66 (1H, s, arom H), 7.6 (1H, d, 8.0 Hz, arom H), 7.4 (1H, d, 7.8 Hz arom H), 2.66 (2H, t, 6.8 Hz, CH2SO3H), 2.32 (3H, s, 2-CH3), 2.10-1.78 (2H, m, CH2), 1.53-1.26 (2H, m, CH2), 1.31 (3H, s, 3-CH3), 0.83-0.41 (2H, m, CH2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09110069B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-8eddc7af58b74b26b2a790c2028d2814
Quellennotizuspto-grants-2015_08