تفاعل #2075720

ord-82e5e5b893f64733892345aa058b6510

معادلة التفاعل

[Li][CH2]CCC
n-butyllithium
Fc1cccc(Cl)c1F
1-chloro-2,3-difluorobenzene
CC(C)OB1OC(C)(C)C(C)(C)O1
2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CC1(C)OB(c2ccc(Cl)c(F)c2F)OC1(C)C
title compound
CC1(C)OB(c2ccc(Cl)c(F)c2F)OC1(C)C
2-(4-Chloro-2,3-difluorophenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to ambient temperature
  2. 2
    استخلاصand the organic phase was extracted twice with water
  3. 3
    استخلاصThe product was then extracted with ethyl acetate
  4. 4
    أخرىThe organic phase was dried
  5. 5
    تركيزconcentrated under vacuum

الإجراء التجريبي

A 2.5 M solution of n-butyllithium (2.69 ml, 6.73 mmol) in hexanes was added dropwise to a solution of 1-chloro-2,3-difluorobenzene (1 g, 6.73 mmol) in THF (25 mL) cooled to −78° C. After 45 min at −78° C., 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.253 g, 6.73 mmol) was added dropwise after which the reaction mixture was allowed to warm to ambient temperature. The reaction mixture was diluted with water and ethyl acetate; and the organic phase was extracted twice with water. The aqueous extracts were combined and acidified with 12N HCl to pH 3. The product was then extracted with ethyl acetate. The organic phase was dried and concentrated under vacuum to yield the title compound as an oil product (0.93 g, 50% yield): 1H NMR (CDCl3): δ 7.42 (m, 1H), 7.17 (m, 1H), 1.37 (s, 12H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07642220B2uspto-grants-2010_01