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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 982858Erstellt: 26. Oktober 2026

Methyl Anthranilate → Methyl 2-(3-oxobutanoylamino)benzoate

https://huagongshe.com/reaction/982858

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl AnthranilateHCID 8635—
EduktDiketeneHCID 12661—
EduktEthyl acetate hexaneHCID 21226206—
KatalysatorTriethylamineHCID 8471—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 2-(3-oxobutanoylamino)benzoateHCID 45932478%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A solution of 2-amino-benzoic acid methyl ester (1.51 g, 10 mmol) and triethylamine (97.2 mmol/ml, 0.0194 mL, 0.14 mmol, 0.014 eq) in toluene (4 mL) was heated to 60° C. and then a solution of 4-methylene-oxetan-2-one (0.84 g, 10 mmol) in toluene (2 ml) was added to the solution over 15 minutes. The reaction was heated at 80° C. for 6 hours and then at 50° C. for 16 hours. Progress of the reaction was monitored by TLC (silica gel, hexane-ethyl acetate (7:3 v/v)), analytical HPLC and LCMS and upon its completion the mixture was partitioned between ethyl acetate and aqueous hydrochloric acid (1 N). The organic layer was washed with water, saturated sodium bicarbonate, water and then brine, dried over Na2SO4 and concentrated to give an orange solid. The solid was crystalized from methylene chloride/ethyl acetate and hexane to provide 2-(3-oxo-butanoylamino)-benzoic acid methyl ester (1.83 g, 78%) as large colorless prisms, mp 81-83° C. (lit., mp 79-80° C.). LCMS MH+ 235.6.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06861419B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-119fb4a04e6b4075b6959d8d2236b273
Quellennotizuspto-grants-2005_03