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HRID 407131Erstellt: 25. Oktober 2026

Methyl chloroformate → 2,4-Di-tert-butylphenyl methyl carbonate

https://huagongshe.com/reaction/407131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl chloroformateHCID 6586—
Edukt2,4-Di-tert-butylphenolHCID 7311—
EduktTriethylamineHCID 8471—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,4-Di-tert-butylphenyl methyl carbonateHCID 59544152—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Methyl chloroformate (58 mL, 750 mmol) was added dropwise to a solution of 2,4-di-tert-butyl-phenol (103.2 g, 500 mmol), Et3N (139 mL, 1000 mmol) and DMAP (3.05 g, 25 mmol) in dichloromethane (400 mL) cooled in an ice-water bath to 0° C. The mixture was allowed to warm to room temperature while stirring overnight, then filtered through silica gel (approx. 1 L) using 10% ethyl acetate-hexanes (˜4 L) as the eluent. The combined filtrates were concentrated to yield carbonic acid 2,4-di-tert-butyl-phenyl ester methyl ester as a yellow oil (132 g, quant.). 1H NMR (400 MHz, DMSO-d6) δ 7.35 (d, J=2.4 Hz, 1H), 7.29 (dd, J=8.5, 2.4 Hz, 1H), 7.06 (d, J=8.4 Hz, 1H), 3.85 (s, 3H), 1.30 (s, 9H), 1.29 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754224B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-fd00f0a7734e440a953a597e5fdf24e6
Quellennotizuspto-grants-2014_06