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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72931Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-(Isopropylthio)-3-methylbenzoic acid

https://huagongshe.com/reaction/72931

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Bromo-3-methylbenzoic acidHCID 82131—
EduktIsopropyl propyl disulfideHCID 118529—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium HydroxideHCID 14798—
Produkt4-(Isopropylthio)-3-methylbenzoic acidHCID 5855092635,8%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Butyllithium (16 mL of 1.6 M, 25.6 mmol) was added dropwise to a mixture of 4-bromo-3-methyl-benzoic acid (2.5 g, 11.6 mmol) and THF (63 mL) at −78° C. The reaction mixture was allowed to stir at −78° C. for 30 minutes before a solution of 2-isopropyldisulfanylpropane (1.7 g, 11.6 mmol) in THF (2 mL) was added dropwise. The mixture was allowed to stir at −78° C. for 30 minutes, then 30 minutes at room temperature. The reaction mixture was then diluted with 1M aqueous sodium hydroxide (100 mL). The organic layer was discarded and the aqueous layer was acidified with 4M aqueous hydrochloric acid. The aqueous layer was then extracted 3 times with ethyl acetate. The combined extracts were dried over sodium sulfate and concentrated in vacuo. The crude material was purified by silica gel column chromatography using a gradient of 0-5% MeOH in dichloromethane to give 4-(isopropylthio)-3-methylbenzoic acid (873 mg, 18%). MS m/z calc. 210.3. Found 211.2 (M+1)+. Retention time: 2.32 minutes (3 min run).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828996B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-9afdff4de9624df2841f718aadf77f50
Quellennotizuspto-grants-2014_09