Pyridine → Chloromethyl 3-methylbutyl carbonate

3-Methyl-1-butanol (4.4 g) was dissolved in dichloromethane (75 ml) and pyridine (4.0 g) was added to it. The reaction mixture was cooled in an ice bath and chloromethyl chloroformate (6.5 g) was added to it with stirring. The cooling bath was removed and the reaction mixture was stirred at room temperature for 16 hours. The dichloromethane solution was washed with water thrice and once with brine. The organic layer was dried over sodium sulfate and evaporated to furnish a colorless oil of desired product weighing 10.7 g which was the pure chloromethyl isopentyl carbonate. NMR (CDCl3) δ 0.95 (6H, d, J=5 Hz, CH(CH3)2), 1.66 (3H, m, CH2 and CH), 4.28 (2H, t, J=7 Hz, OCH2CH2) and 5.73 (2H, s, OCH2Cl). IR (film) 2950, 1783, 1265 cm-1.

1. temperatureThe reaction mixture was cooled in an ice bath
2. customThe cooling bath was removed
3. stirringthe reaction mixture was stirred at room temperature for 16 hours
4. washThe dichloromethane solution was washed with water thrice and once with brine
5. dry with materialThe organic layer was dried over sodium sulfate
6. customevaporated

ORD record

ord-6ede1b901447430681bc22c35136c058

Source dataset

uspto-grants-1984_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04426391