Reacción #326221

Ecuación de reacción

LDA

103b

t-Butyl 1-(4-bromo-butyl)-cyclopropanecarboxylate

t-butyl cyclopropanecarboxylate

1-bromo-4-chlorobutane

→

Compound 104a

t-Butyl 1-(4-chlorobutyl)-1-cyclopropanecarboxylate

Condiciones de reacción

Tratamiento posterior

1. 1
   Otroto give
2. 2
   Otroafter purification
3. 3
   workup.DISTILLATIONby fractional distillation under reduced pressure, 104a (10.73 g 52%) as a colorless oil
4. 4
   OtroT=57-61° C. (p=0.001 mbar)

Procedimiento

Compound 104a was prepared, likewise the procedure described for 103b, starting from t-butyl cyclopropanecarboxylate (Kohlrausch, K. W. F. et al. Z Elektrochem. Angew. Phys. Chem, 1937, 43, 282-285) (12.5 g, 88 mmol), 1-bromo-4-chlorobutane (13.7 mL, 117 mmol) and LDA (prepared from BuLi (2.5M in hexanes, 37 mL, 92.5 mmol) and iPr2NH (12.3 mL, 88 mmol, distilled from NaOH)) to give, after purification by fractional distillation under reduced pressure, 104a (10.73 g 52%) as a colorless oil. bp: T=57-61° C. (p=0.001 mbar). 1H NMR: δ 3.52 (t, J=6.6 Hz, 2H), 1.76 (quintet, J=6.8 Hz, 2H), 1.64-1.54 (m, 2H), 1.51-1.46 (m, 2H), 1.42 (s, 9H), 1.12 (dd, J=6.6, 3.9 Hz, 2H), 0.60 (dd, J=6.6, 3.9 Hz, 2H). 13C NMR: δ 173.9, 80.0, 45.1, 33.6, 32.9, 28.2 (3×), 25.3, 24.2, 15.4 (2×). HRMS calcd for C12H22ClO2 (MH+): 233.1308, found: 233.1308.

Fuente