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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1181396Erstellt: 26. Oktober 2026

Carbamate → Benzenemethanamine, N-methyl-4-(trifluoromethyl)-

https://huagongshe.com/reaction/1181396

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbamateHCID 276—
EduktAmmonium ChlorideHCID 25517—
Edukt4-(Trifluoromethyl)benzylamineHCID 76804—
EduktCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzenemethanamine, N-methyl-4-(trifluoromethyl)-HCID 485420—

Reaktionsschritte

A mixture of 4-(trifluoromethyl)benzylamine (1.0 mL, 7.02 mmol) and di-tert-butyl carbonate (1.68 g, 7.72 mmol) in CH2Cl2 (10 mL) was stirred for 1 hour. The reaction mixture was poured into saturated aqueous ammonium chloride solution, extracted with CH2Cl2 and the organic layers were combined, dried over MgSO4 and concentrated in vacuo to give a white crystalline solid. To a solution of the crude carbamate (1.00 g, 3.61 mmol) in THF (20 mL) in a room temperature water bath, was added LiAlH4 (0.69 g, 18.1 mmol) portion-wise over 10 minutes. The reaction was then heated at reflux for 4 hours. The reaction was cooled in ice and quenched by the addition of water (1.6 mL) and NaOH (2N, 1.3 mL). The grey slurry was filtered and washed with MeOH. The MeOH was removed in vacuo and the crude product taken up in CH2Cl2 and dried over MgSO4 and concentrated in vacuo. Purification by flash column chromatography eluting with 5-10% MeOH in CH2Cl2 plus 1% NH3 solution (2N in MeOH) afforded the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07285563B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-0fd7b82f0ea3401aac99be59d275d7d7
Quellennotizuspto-grants-2007_10