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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 383346Erstellt: 26. Oktober 2026

Methyl chloroformate → 2-Bromo-4-tert-butylphenyl methyl carbonate

https://huagongshe.com/reaction/383346

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl chloroformateHCID 6586—
EduktTriethylamineHCID 8471—
Edukt2-Bromo-4-tert-butylphenolHCID 75147—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Bromo-4-tert-butylphenyl methyl carbonateHCID 5939494490,4%

Reaktionsschritte

2-Bromo-4-tert-butyl phenol (15.0 g, 65.5 mmol) and DMAP (400 mg, 3.3 mmol) was dissolved in dichloromethane (75 mL) and triethylamine (18.25 mL, 130.9 mmol), cooled to 0° C., then treated with methyl chloroformate (7.6 mL, 98.2 mmol) and allowed to warm to room temperature over 2 h. The reaction was quenched with water and the layers separated. The aqueous layer was extracted with dichloromethane and the combined organic extracts dried over Na2SO4. The solution was filtered and concentrated in vacuo to yield an oil that was purified by silica gel chromatography (20% ethyl acetate/hexane) to yield 2-bromo-4-tert-butylphenyl methyl carbonate (17 g, 90% yield). 1H NMR (400.0 MHz, DMSO-d6) δ 7.67 (d, J=2.3 Hz, 1H), 7.47 (dd, J=2.3, 8.5 Hz, 1H), 7.33 (d, J=8.5 Hz, 1H), 3.86 (s, 3H), 1.29-1.26 (m, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367660B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-a8fa18584d9346c4bffae1f5e39f8bb5
Quellennotizuspto-grants-2013_02