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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579596Erstellt: 24. Oktober 2026

1,2-Dichloroethane → 4-(4-Chlorophenyl)-cyclohexanecarboxylic acid, methoxy-methyl amide

https://huagongshe.com/de/reaction/579596

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktTriethylamineHCID 8471—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Edukt4-(4-Chlorophenyl)cyclohexane-1-carboxylic acidHCID 2735792—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(4-Chlorophenyl)-cyclohexanecarboxylic acid, methoxy-methyl amideHCID 88577128—

Reaktionsschritte

EDC (3.21 g, 16.8 mmol) was added portionwise to a stirred solution of 4-(4-chlorophenyl)-cyclohexanecarboxylic acid (2.0 g, 8.4 mmol), DMAP (5 mg), HOBt (5 mg) and N,O-dimethylhydroxylamine hydrochloride (1.63 g, 16.8 mmol) in dichloromethane (40 mL). Triethylamine (3.4 g, 4.7 mL, 33.5 mmol) was added dropwise, and the reaction mixture was stirred at room temperature. After stirring overnight the reaction mixture was poured into water and extracted with ethyl acetate (3×). The combined organic phase was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give 4-(4-chlorophenyl)-cyclohexanecarboxylic acid, methoxy-methyl amide as a colorless oil (1.85 g. 78%); MS (+CI): m/z for C15H20ClNO2: expected 281.1. found 282.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040703B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-b3567bb806dc48f794504e860688111f
Quellennotizuspto-grants-2015_05