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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1496695Erstellt: 25. Oktober 2026

Methanol → Methyl alpha-phenylbenzeneacetate

https://huagongshe.com/reaction/1496695

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDiphenylacetic AcidHCID 8333—
EduktOxalyl chlorideHCID 65578—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl alpha-phenylbenzeneacetateHCID 7701998,7%

Reaktionsschritte

To a 500 mL three-opening flask were added 2,2-diphenylacetic acid (20 g, 94 mmol) and 200 mL dichloromethane. After stirring, 1 mL DMF was added. To the mixture was slowly added oxalyl chloride (13.16 g, 104 mmol) dropwisely in an ice bath. The reaction was conducted at 25° C. After the completion of reaction, the mixture was evaporated under reduced pressure to remove oxalyl chloride. To the reaction flask were slowly added dichloromethane (100 mL) and anhydrous methanol (3.61 g, 113 mmol) dropwisely under cooling in an ice bath respectively. The reaction was conducted at 25° C. After the completion of reaction, the reaction solution was washed with a saturated aqueous NaCl solution. The organic phase was dried over sodium sulfate, and filtered by suction. The filtrate was evaporated to dryness to produce methyl 2,2-diphenylacetate (21 g) in a yield of 98.7%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09198902B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-6421fe09785044cd9ad76a4245e96c0f
Quellennotizuspto-grants-2015_12