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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1282867Erstellt: 25. Oktober 2026

Triethylamine → N-t-butoxycarbonyl-p-hydroxymethylphenylglycine

https://huagongshe.com/reaction/1282867

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktCarbonazidic acid, 1,1-dimethylethyl esterHCID 61256—
Eduktp-HydroxymethylphenylglycineHCID 53754844—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-t-butoxycarbonyl-p-hydroxymethylphenylglycineHCID 2056472963%

Reaktionsschritte

To a solution of p-hydroxymethylphenylglycine (8.0 g, 0.044 mole) and triethylamine (8.8 g., 0.087 mole) in 160 ml water was added t-butoxycarbonyl azide (6.95 g., 0.049 mole) dissolved in 120 ml tetrahydrofuran. After stirring overnight at room temperature, the reaction mixture was washed twice with 200 ml. portions of ether. The aqueous layer was covered with ether and in an ice bath was acidified to pH 3-3.5 with 3N hydrochloric acid. The acidic solution was extracted three times with 200 ml portions of ether. The combined ether layers were washed with saturated sodium chloride solution, dried, and the ether evaporated under reduced pressure. The resulting oil was triturated with chloroform-hexane and the solid filtered off to give N-t-butoxycarbonyl-p-hydroxymethylphenylglycine (7.74 g, 63 percent yield), m.p. 139°-141.5° (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03972919
Quelldatensatzuspto-grants-1976_08
ORD IDord-012d61a002d940c3a5eef9737d53a4cd
Quellennotizuspto-grants-1976_08