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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 854941Erstellt: 24. Oktober 2026

Hydrochloric Acid → HCID 20351850, Verbindung

https://huagongshe.com/de/reaction/854941

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethanolHCID 887—
Edukt2-Amino-3-bromo-5-methylbenzoic acidHCID 2774400—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 20351850HCID 2035185051%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The 2-amino-3-bromo-5-methylbenzoic acid (20.0 g, 86.0 mmol) was dissolved in tetrahydrofuran (200 ml) and cooled to 0° C. A solution of borane dimethylsulfide complex (15.6 mL, 156.0 mmol) was dissolved in tetrahydrofuran (40 mL) and added dropwise. The solution was kept at 0° C. for an additional 30 minutes, warmed to room temperature for 2 h and finally refluxed for 16 h. The solution was cooled to room temperature and methanol (10 mL) added slowly to control the gas evolution. The solution was stirred for 30 minutes at room temperature and 1 N hydrochloric acid added. The solution was stirred for 3 h and solvent removed to a volume of about 100 mL. Water (200 mL) was added and the solution extracted with diethylether (200 mL). The aqueous layer was collected, adjusted to pH=12 with 1N sodium hydroxide which formed a solid in the solution. The solid was collected, dissolved in ethyl acetate (100 mL), dried over sodium sulfate and solvent removed at reduced pressure. The (2-amino-3-bromo-5-methylphenyl)methanol (9.5 g, 43.9 mmol) was obtained as a off white solid. (51% yield): HRMS m/z 216.0047; calcd for M+H 216.0024.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07259266B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-526817bc5f8a4863b8f18c4c3d9c1110
Quellennotizuspto-grants-2007_08